The United States of America as represented by the Department of Health and Human Services

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C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor 10
A61K 38/00 - Medicinal preparations containing peptides 8
C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical 8
C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids 7
G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor 6
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Found results for  patents

1.

HIV RNA VACCINES

      
Application Number 18771978
Status Pending
Filing Date 2024-07-12
First Publication Date 2025-03-06
Owner
  • ModernaTX, Inc. (USA)
  • The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Lusso, Paolo
  • Zhang, Peng
  • Narayanan, Elisabeth
  • Elbashir, Sayda Mahgoub

Abstract

Provided herein are methods and compositions for inducing in a subject a broad neutralizing antibody response to human immunodeficiency virus (HIV) infection.

IPC Classes  ?

  • A61K 39/21 - Retroviridae, e.g. equine infectious anemia virus
  • A61K 39/00 - Medicinal preparations containing antigens or antibodies
  • A61K 39/39 - Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants

2.

HIV RNA vaccines

      
Application Number 17439198
Grant Number 12070495
Status In Force
Filing Date 2020-03-13
First Publication Date 2022-08-04
Grant Date 2024-08-27
Owner
  • ModernaTX, Inc. (USA)
  • The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Lusso, Paolo
  • Zhang, Peng
  • Narayanan, Elisabeth
  • Elbashir, Sayda Mahgoub

Abstract

Provided herein are methods and compositions for inducing in a subject abroad neutralizing antibody response to human immunodeficiency virus (HIV) infection.

IPC Classes  ?

  • A61K 39/21 - Retroviridae, e.g. equine infectious anemia virus
  • A61K 39/39 - Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
  • A61K 39/00 - Medicinal preparations containing antigens or antibodies

3.

CORONAVIRUS RNA VACCINES AND METHODS OF USE

      
Application Number US2021032609
Publication Number 2021/159130
Status In Force
Filing Date 2021-05-14
Publication Date 2021-08-12
Owner
  • MODERNATX, INC. (USA)
  • THE UNITED STATES OF AMERICA, as represented by THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (USA)
Inventor
  • Bennett, Hamilton
  • Stewart-Jones, Guillaume
  • Narayanan, Elisabeth
  • Carfi, Andrea
  • Metkar, Mihir
  • Presnyak, Vladimir
  • Graham, Barney S.
  • Corbett, Kizzmekia S.

Abstract

The disclosure relates to SARS-CoV-2 messenger ribonucleic acid (mRNA) vaccine compositions as well as methods of using the vaccines.

IPC Classes  ?

  • A61K 39/215 - Coronaviridae, e.g. avian infectious bronchitis virus

4.

ARYL HYDANTOIN HETEROCYCLES AND METHODS OF USE

      
Document Number 03165120
Status Pending
Filing Date 2021-01-20
Open to Public Date 2021-07-29
Owner
  • UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (USA)
  • GEORGIA TECH RESEARCH CORPORATION (USA)
Inventor
  • Gryder, Berkley E.
  • Oyelere, Adegboyega K.
  • Tapadar, Subhasish
  • Strope, Jonathan D.
  • Figg, Sr. William Douglas

Abstract

Disclosed is a compound of formula (I) in which R1, R2, R3, X1, X2, X2', X3, X4, ring A, m, n, and o are as described herein. The compound of formula (I) is useful for treating a disorder associated with androgen receptor malfunction, such as a hyperproliferative disorder, in a subject in need thereof.

IPC Classes  ?

  • A61K 31/4192 - 1,2,3-Triazoles
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61P 35/00 - Antineoplastic agents
  • C07D 401/14 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
  • C07D 403/10 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a carbon chain containing aromatic rings

5.

ZIKA VIRAL ANTIGEN CONSTRUCTS

      
Application Number EP2017079343
Publication Number 2018/091540
Status In Force
Filing Date 2017-11-15
Publication Date 2018-05-24
Owner
  • GLAXOSMITHKLINE BIOLOGICALS SA (Belgium)
  • THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (USA)
Inventor
  • Dowd, Kimberly
  • Graham, Barney S.
  • Ko, Sung-Youl
  • Kong, Wing-Pui
  • Mascola, John
  • Pierson, Theodore
  • Sharma, Mayuri
  • Yu, Dong

Abstract

Compounds useful as components of immunogenic compositions for the induction of an immunogenic response in a subject against viral infection, methods for their use in treatment, and processes for their manufacture are provided herein. The compounds comprise a nucleic acid construct comprising a sequence which encodes a Zika virus antigen.

IPC Classes  ?

6.

Antifungal compound process

      
Application Number 15126420
Grant Number 10017494
Status In Force
Filing Date 2015-03-19
First Publication Date 2017-04-06
Grant Date 2018-07-10
Owner
  • Mycovia Pharmaceuticals, Inc. (USA)
  • The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Hoekstra, William J.
  • Yates, Christopher M.
  • Behnke, Mark
  • Alimardanov, Asaf
  • David, Scott A.
  • Fry, Douglas Franklin

Abstract

The present invention relates to a process for preparing compound 1 that is useful as an antifungal agent. In particular, the invention seeks to provide new methodology for preparing compound 1 and substituted derivatives thereof.

IPC Classes  ?

  • C07D 405/06 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • C07D 213/50 - Ketonic radicals
  • C07D 213/30 - Oxygen atoms
  • C07D 401/06 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • C07D 213/38 - Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
  • C07D 213/56 - Amides

7.

N-substituted indenoisoquinolines and syntheses thereof

      
Application Number 13317153
Grant Number 08829022
Status In Force
Filing Date 2011-10-11
First Publication Date 2012-04-26
Grant Date 2014-09-09
Owner
  • Purdue Research Foundation (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Cushman, Mark S.
  • Morrell, Andrew E.
  • Nagarajan, Muthukaman
  • Pommier, Yves G.
  • Agama, Keli K.
  • Antony, Smitha

Abstract

N-Substituted indenoisoquinoline compounds, and pharmaceutical formulations of N-substituted indenoisoquinoline compounds are described. Also described are processes for preparing N-substituted indenoisoquinoline compounds. Also described are methods for treating cancer in mammals using the described N-substituted indenoisoquinoline compounds or pharmaceutical formulations thereof.

IPC Classes  ?

  • C07D 221/18 - Ring systems of four or more rings
  • A61K 31/473 - QuinolinesIsoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
  • A61K 31/4741 - QuinolinesIsoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline

8.

Human gene related to but distinct from EGF receptor gene

      
Application Number 07110791
Grant Number 07838216
Status In Force
Filing Date 1987-10-21
First Publication Date 2010-11-23
Grant Date 2010-11-23
Owner The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • King, C. Richter
  • Kraus, Matthias H.
  • Aaronson, Stuart A.

Abstract

The isolation, cloning and characterization of a human gene related to but distinct from EGF receptor gene has been described. Nucleotide sequence of the gene and amino acid sequence of the polypeptide encoded by the gene have been determined. The use of the nucleic acid probes and antibodies having specific binding affinity with said polypeptide for diagnostic and therapeutic purposes have also been described.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

9.

QUINONE DERIVATIVE 2,3-DIMETHOXY-5-METHYL-6-(10-HYDROXYDECYL)-1,4-BENZOQUINONE FOR THE TREATMENT OF PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS

      
Application Number EP2009009148
Publication Number 2010/124713
Status In Force
Filing Date 2009-12-18
Publication Date 2010-11-04
Owner
  • SANTHERA PHARMACEUTICALS (SCHWEIZ) AG (Switzerland)
  • THE UNITED STATES OF AMERICA as represented by THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (USA)
Inventor
  • Meier, Thomas
  • Bielekova, Bibiana
  • Mcfarland, Henry, F.

Abstract

The present invention relates to pharmaceuticals and uses thereof directed to the curative treating or preventing of Primary Progressive Multiple Sclerosis. (PP-MS), by using 2, 3-dιmethoxy-5-methyl-6- (10-hydroxydecyl) -1, 4-benzoquιnone (Idebenone) as the active agent.

IPC Classes  ?

  • A61K 31/122 - Ketones having the oxygen atom directly attached to a ring, e.g. quinones, vitamin K1, anthralin
  • A61P 25/00 - Drugs for disorders of the nervous system

10.

Method, system and computer program method for detection of pathological fluctuations of physiological signals to diagnose human illness

      
Application Number 12724162
Grant Number 08615291
Status In Force
Filing Date 2010-03-15
First Publication Date 2010-09-16
Grant Date 2013-12-24
Owner
  • National Institutes of Health (NIH) (USA)
  • The United States of America as Represented by the Department of Health and Human Services (USA)
Inventor
  • Moorman, Randall
  • Lake, Douglas E.
  • Flower, Abigail
  • Delos, John B.

Abstract

Method, system, and computer program method for detecting pathological fluctuations of physiological signals to diagnose human illness. The method comprises performing a sliding window analysis to find sequences in physiological signal data that match amplitude- and duration-adjusted versions of a template function to within a specified tolerance.

IPC Classes  ?

  • A61B 5/04 - Measuring bioelectric signals of the body or parts thereof

11.

Use of lymphocytes to measure anthrax lethal toxin activity

      
Application Number 11399003
Grant Number 07803565
Status In Force
Filing Date 2006-04-05
First Publication Date 2010-09-09
Grant Date 2010-09-28
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Frucht, David M.
  • Fang, Hui

Abstract

+ T-cell can be used to determine an amount of lymphocyte-associated anthrax lethal toxin activity present. Methods of using isolated lymphocytes to identify anthrax therapeutic agents and to determine the efficacy of a potential anthrax therapeutic are disclosed. Methods are also provided for diagnosing and treating anthrax infections.

IPC Classes  ?

  • G01N 33/00 - Investigating or analysing materials by specific methods not covered by groups
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor
  • G01N 33/569 - ImmunoassayBiospecific binding assayMaterials therefor for microorganisms, e.g. protozoa, bacteria, viruses
  • G01N 33/573 - ImmunoassayBiospecific binding assayMaterials therefor for enzymes or isoenzymes
  • C12N 5/07 - Animal cells or tissues
  • C12N 5/16 - Animal cells

12.

Deletion of the beta 20-21 loop in HIV gp120 exposes the CD4 binding site for improved antibody binding and antibody induction

      
Application Number 12714085
Grant Number 08628782
Status In Force
Filing Date 2010-02-26
First Publication Date 2010-08-26
Grant Date 2014-01-14
Owner The United States of America, as Represented by the Department of Health and Human Services (USA)
Inventor Berkower, Ira

Abstract

Disclosed herein are isolated immunogens including variant gp120 polypeptides. In an example, a variant gp120 polypeptide includes a deletion of at least 8 consecutive residues of the fourth conserved loop (C4) between residues 419 and 434 of gp120 according to HXB2 numbering. Also provided are isolated nucleic acid molecules encoding the disclosed isolated immunogens. In an example, an isolated nucleic acid molecule further includes a nucleic acid molecule encoding a hepatitis B surface antigen or a variant thereof. Compositions including the isolated immunogens including variant gp120 polypeptides are also disclosed. In some examples, a composition further includes a carrier protein, such as a hepatitis B surface antigen or a variant thereof (natural or recombinant). Viral-like particles are also provided including any of the disclosed isolated immunogens or compositions. Also disclosed are uses of these variant gp120 polypeptides and nucleic acids encoding variant polypeptides, such as to induce an immune response to HIV-1.

IPC Classes  ?

  • A61K 39/21 - Retroviridae, e.g. equine infectious anemia virus

13.

Spatially selective fixed-optics multicolor fluorescence detection system for a multichannel microfluidic device, and method for detection

      
Application Number 11993852
Grant Number 07924425
Status In Force
Filing Date 2006-06-26
First Publication Date 2010-07-01
Grant Date 2011-04-12
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Morgan, Nicole Y.
  • Smith, Paul
  • Wellner, Ed

Abstract

A system for spatially selective, fixed-optics fluorescence detection in a multichannel polymeric microfluidic device, and a method for performing spatially selective, fixed-optics fluorescence detection.

IPC Classes  ?

  • G01N 21/00 - Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light

14.

Staphylococcus

      
Application Number 12631253
Grant Number 08211445
Status In Force
Filing Date 2009-12-04
First Publication Date 2010-05-13
Grant Date 2012-07-03
Owner The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Otto, Michael
  • Wang, Rong

Abstract

staphylococcus in a subject.

IPC Classes  ?

15.

SCGB3A2 as a growth factor and anti-apoptotic agent

      
Application Number 12442927
Grant Number 08133859
Status In Force
Filing Date 2007-09-27
First Publication Date 2010-04-15
Grant Date 2012-03-13
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Kimura, Shioko
  • Kurotani, Reiko

Abstract

The present disclosure is generally related to methods of using the secretory protein SCGB3A2 for promoting lung development and treating lung disease. Some embodiments are, for example, methods for treating and inhibiting the development of neonatal respiratory distress. Other embodiments are methods of promoting lung development in damaged or diseased lungs. Also disclosed are methods for inhibiting lung damage due to anti-cancer agents.

IPC Classes  ?

16.

Method of preparing macromolecular contrast agents and uses thereof

      
Application Number 12513813
Grant Number 08288530
Status In Force
Filing Date 2007-11-06
First Publication Date 2010-03-04
Grant Date 2012-10-16
Owner The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Brechbiel, Martin W.
  • Xu, Heng

Abstract

Disclosed are methods of preparing a macromolecular conjugated ligand and a metal complex thereof. The metal complex is targeted for use as a contrast agent, for example, in MRI. The method of preparing a macromolecular conjugated ligand comprises: (a) providing a compound of formula (I) wherein R, A, and Pg are as defined herein, (b) reacting the compound of formula (I) with a macromolecular compound (e.g., dendrimer) in an organic solvent medium which is substantially free of water to obtain a macromolecular conjugated compound, and (c) removing the carboxyl-protecting groups to obtain a carboxyl-deprotected macromolecular conjugated compound. The metal complex can be prepared by reacting the carboxyl-deprotected macromolecular conjugated compound with an ion (e.g., Gd(III)). Also disclosed are two carboxyl-protected 1B4M-DTPA intermediate compounds.

IPC Classes  ?

  • C07D 403/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group containing two hetero rings linked by a chain containing hetero atoms as chain links
  • C07D 207/46 - Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
  • C07D 207/40 - 2,5-Pyrrolidine-diones
  • C07D 257/02 - Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
  • C07C 229/00 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton

17.

Boris isoforms and methods of detecting and treating disease

      
Application Number 12439063
Grant Number 08206933
Status In Force
Filing Date 2007-08-30
First Publication Date 2010-01-28
Grant Date 2012-06-26
Owner The United States of America, as represented by the Department of Health and Human Services (USA)
Inventor
  • Lobanenkov, Victor V.
  • Pugacheva, Elena
  • Loukinov, Dmitri

Abstract

A method of detecting a proliferative disease, such as a disease associated with the abnormal expression of BORIS, in a mammal comprising testing for the expression of a BORIS isoform in the tissue of a mammal that does not express BORIS in the absence of disease, as well as a method of treating or preventing such a disease, isolated or purified BORIS isoform polypeptides and nucleic acids, and kits and arrays comprising same.

IPC Classes  ?

  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

18.

Inductive decoupling of a RF coil array

      
Application Number 12296417
Grant Number 07932721
Status In Force
Filing Date 2007-04-06
First Publication Date 2009-11-26
Grant Date 2011-04-26
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Nascimento, George
  • Silva, Afonso C.

Abstract

An apparatus for imaging includes: a radio frequency (RF) coil array having a first RF coil and at least one additional RF coil, where the RF coil array is adapted to generate an image signal; a preamplifier having an input impedance, where the preamplifier is adapted to receive the image signal from the first RF coil; and a transformer to couple the first RF coil to the preamplifier, where impedance of the transformer is adapted to match the input impedance of the preamplifier.

IPC Classes  ?

  • G01V 3/00 - Electric or magnetic prospecting or detectingMeasuring magnetic field characteristics of the earth, e.g. declination or deviation

19.

Recombinant expression vectors comprising a human codon-optimized marburg virus (MARV) angola glycoprotein gene insert and method of immunization employing said vector

      
Application Number 11662869
Grant Number 08101739
Status In Force
Filing Date 2005-09-27
First Publication Date 2009-09-17
Grant Date 2012-01-24
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Sullivan, Nancy
  • Chakrabarti, Bimal
  • Yang, Zhi-Yong
  • Pau, Maria Grazia
  • Goudsmit, Jaap
  • Nabel, Gary

Abstract

The invention is related to a nucleic acid molecule comprising a polynucleotide encoding a modified filovirus glycoprotein (GP) having at least one amino acid change located in a relatively conserved region of said GP that decreases in vitro cytotoxicity and retains immunogenicity when compared to in vitro cytotoxicity and immunogenicity of a wild type filovirus GP, and related modified filovirus GPs, plasmid DNAs, recombinant viruses, adenoviruses, pharmaceutical compositions, vaccine compositions, antibodies that are specifically reactive with the modified filovirus GPs, and related methods of making and using the same.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • A61K 39/12 - Viral antigens

20.

Human monoclonal antibodies against Hendra and Nipah viruses

      
Application Number 11886307
Grant Number 07988971
Status In Force
Filing Date 2005-11-04
First Publication Date 2009-08-27
Grant Date 2011-08-02
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. (USA)
Inventor
  • Dimitrov, Dimiter S.
  • Zhongyu, Zhu
  • Broder, Christopher C.

Abstract

The present invention relates to monoclonal antibodies that bind or neutralize Hendra or Nipah virus. The invention provides such antibodies, fragments of such antibodies retaining Hendra or Nipah virus-binding ability, fully human antibodies retaining Hendra or Nipah virus-binding ability, and pharmaceutical compositions including such antibodies. The invention further provides for isolated nucleic acids encoding the antibodies of the invention and host cells transformed therewith. Additionally, the invention provides for prophylactic, therapeutic, and diagnostic methods employing the antibodies and nucleic acids of the invention.

IPC Classes  ?

  • A61K 39/42 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum viral
  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • A61K 39/12 - Viral antigens
  • A61K 39/155 - Paramyxoviridae, e.g. parainfluenza virus
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies
  • A61K 39/275 - Poxviridae, e.g. avipoxvirus

21.

Multi-domain amphipathic helical peptides and methods of their use

      
Application Number 11577259
Grant Number 07572771
Status In Force
Filing Date 2007-04-13
First Publication Date 2009-08-11
Grant Date 2009-08-11
Owner The United States of America as represented by the Departments of Health and Human Services (USA)
Inventor
  • Remaley, Alan T.
  • Demosky, Stephen J.
  • Stonik, John A.
  • Amar, Marcele J. A.
  • Neufeld, Edward B.
  • Brewer, H. Bryan
  • Thomas, Fairwell

Abstract

Disclosed herein are peptides or peptide analogs with multiple amphipathic α-helical domains that promote lipid efflux from cells via an ABCA1-dependent pathway. Also provided herein are methods of using multi-domain amphipathic α-helical peptides or peptide analogs to treat or inhibit dyslipidemic disorders. Methods for identifying non-cytotoxic peptides that promote ABCA1-dependent lipid efflux from cells are also disclosed herein.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides
  • C07K 5/00 - Peptides having up to four amino acids in a fully defined sequenceDerivatives thereof

22.

MRI navigator methods and systems

      
Application Number 10244903
Grant Number 07561909
Status In Force
Filing Date 2002-09-16
First Publication Date 2009-07-14
Grant Date 2009-07-14
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Pai, Vinay M.
  • Wen, Han

Abstract

Navigator methods are disclosed that are based on detecting a flow-sensitive signal within a subject, and using the position of the signal to track subject motion between imaging sequences. In a disclosed embodiment, the fast-moving blood volume in the left ventricle of the heart is detected and used as a reference point to correct for cardiac motion that results from respiratory motion in a subject. The navigator based on the position of the fast-moving blood volume in the left ventricle may be applied prospectively to shift a subsequent imaging slice to compensate for subject motion, and thereby provide MRI images with increased clarity and resolution.

IPC Classes  ?

  • A61B 5/05 - Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fieldsMeasuring using microwaves or radio waves

23.

Monoclonal antibodies against orthopoxviruses

      
Application Number 12142594
Grant Number 07914788
Status In Force
Filing Date 2008-06-19
First Publication Date 2009-06-18
Grant Date 2011-03-29
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Chen, Zhaochun
  • Earl, Patricia
  • Moss, Bernard
  • Emerson, Suzanne U.
  • Purcell, Robert H.

Abstract

The present invention relates to monoclonal antibodies that bind or neutralize Orthopoxviruses. The invention provides such antibodies, fragments of such antibodies retaining B5 or A33 binding ability, fully human antibodies retaining B5 or A33 binding ability, and pharmaceutical compositions including such antibodies. The invention further provides for isolated nucleic acids encoding the antibodies of the invention and host cells transformed therewith. Additionally, the invention provides for prophylactic, therapeutic, and diagnostic methods employing the antibodies and nucleic acids of the invention.

IPC Classes  ?

  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor

24.

Method of treating inflammatory arthropathies with suppressors of CpG oligonucleotides

      
Application Number 12325106
Grant Number 07951786
Status In Force
Filing Date 2008-11-28
First Publication Date 2009-06-04
Grant Date 2011-05-31
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Klinman, Dennis
  • Zeuner, Rainald
  • Verthelyi, Daniela
  • Gursel, Ihsan
  • Gursel, Mayda

Abstract

The present disclosure relates to oligodeoxynucleotides that suppress an immune response. Methods are disclosed for preventing or treating inflammatory arthropathies by administering a therapeutically effective amount of a suppressive oligodeoxynucleotide.

IPC Classes  ?

  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy

25.

Griffithsin, glycosylation-resistant griffithsin, and related conjugates, compositions, nucleic acids, vectors, host cells, methods of production and methods of use

      
Application Number 11569813
Grant Number 07884178
Status In Force
Filing Date 2005-05-27
First Publication Date 2009-04-09
Grant Date 2011-02-08
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Boyd, Michael R.
  • Mori, Toshiyuki
  • O'Keefe, Barry R.

Abstract

An isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 3, wherein the at least eight contiguous amino acids have anti-viral activity, as well as an isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 3, wherein the at least eight contiguous amino acids have anti-viral activity, and, when the at least eight contiguous amino acids comprise amino acids 1-121 of SEQ ID NO: 3, the at least eight contiguous amino acids have been rendered glycosylation-resistant, a vector comprising such an isolated and purified nucleic acid molecule, a host cell comprising the nucleic acid molecule, optionally in the form of a vector, a method of producing an anti-viral polypeptide or conjugate thereof, the anti-viral polypeptide itself, a conjugate or fusion protein comprising the anti-viral polypeptide, and compositions comprising an effective amount of the anti-viral polypeptide or conjugate or fusion protein thereof. Further provided are methods of inhibiting prophylactically or therapeutically a viral infection of a host.

IPC Classes  ?

  • A61K 49/00 - Preparations for testing in vivo
  • A61K 38/00 - Medicinal preparations containing peptides

26.

Immunogenic peptides and methods of use

      
Application Number 12280534
Grant Number 07910692
Status In Force
Filing Date 2007-02-21
First Publication Date 2009-02-05
Grant Date 2011-03-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Schlom, Jeffrey
  • Tsang, Kwong-Yok
  • Pastan, Ira H

Abstract

The PAGE4 gene is expressed in reproductive tissues, and is expressed in reproductive cancers, such as prostate cancer, uterine cancer, and testicular cancer. Immunogenic PAGE4 polypeptides are disclosed herein, as are nucleic acids encoding the immunogenic PAGE4 polypeptides, vectors including these polynucleotides, and host cells transformed with these vectors. These polypeptides, polynucleotides, vectors, and host cells can be used to induce an immune response to PAGE4. Diagnostic methods to detect PAGE4 are also described.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides
  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy
  • C07K 7/00 - Peptides having 5 to 20 amino acids in a fully defined sequenceDerivatives thereof
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

27.

Peptides of a melanoma antigen and their use in diagnostic, prophylactic, and therapeutic methods

      
Application Number 12195809
Grant Number 07749967
Status In Force
Filing Date 2008-08-21
First Publication Date 2009-01-08
Grant Date 2010-07-06
Owner The United States of America as represented by the Department of Health and Human Services. (USA)
Inventor
  • Hwu, Patrick
  • Lapointe, Rejean
  • Rosenberg, Steven A.
  • Parkhurst, Maria

Abstract

Immunogenic peptides of a melanoma antigen recognized by T cells, designated gp100, bioassays using the peptides to diagnose, assess or prognose a mammal afflicted with cancer, more specifically melanoma or metastatic melanoma, and use of the proteins and peptides as immunogens to inhibit, prevent or treat melanoma.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides
  • C07K 5/00 - Peptides having up to four amino acids in a fully defined sequenceDerivatives thereof

28.

Mutated Anti-CD22 antibodies with increased affinity to CD22-expressing leukemia cells

      
Application Number 12030828
Grant Number 07777019
Status In Force
Filing Date 2008-02-13
First Publication Date 2009-01-01
Grant Date 2010-08-17
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Pastan, Ira
  • Salvatore, Giuliana
  • Beers, Richard
  • Kreitman, Robert J.

Abstract

Recombinant immunotoxins are fusion proteins composed of the Fv domains of antibodies fused to bacterial or plant toxins. RFB4 (Fv)-PE38 is an immunotoxin that targets CD22 expressed on B cells and B cell malignancies. The present invention provides antibodies and antibody fragments that have improved ability to bind the CD22 antigen of B cells and B cell malignancies compared to RFB4. Immunotoxins made with the antibodies and antibody fragments of the invention have improved cytotoxicity to CD22-expressing cancer cells. Compositions that incorporate these antibodies into chimeric immunotoxin molecules that can be used in medicaments and methods for inhibiting the growth and proliferation of leukemia and lymphoma cells.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies

29.

PDE11A mutations in adrenal disease

      
Application Number 12161866
Grant Number 07847078
Status In Force
Filing Date 2007-01-19
First Publication Date 2009-01-01
Grant Date 2010-12-07
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor Stratakis, Constantine A.

Abstract

The invention provides previously uncharacterized variants of PDE11A that are correlated with a newly discovered form of Cushing Syndrome that presents at a young age. The invention also provides methods useful to research, screen for, treat, or prevent diagnose the disease using the PDE11A variants, as well as other methods relating thereto.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • C12N 5/02 - Propagation of single cells or cells in suspensionMaintenance thereofCulture media therefor
  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy

30.

N-substituted indenoisoquinolines and syntheses thereof

      
Application Number 12093398
Grant Number 08053443
Status In Force
Filing Date 2006-11-13
First Publication Date 2008-12-25
Grant Date 2011-11-08
Owner
  • Purdue Research Foundation (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Cushman, Mark S.
  • Morrell, Andrew E.
  • Nagarajan, Muthukaman
  • Pommier, Yves G.
  • Agama, Keli K.
  • Antony, Smitha

Abstract

N-Substituted indenoisoquinoline compounds, and pharmaceutical formulations of N-substituted indenoisoquinoline compounds are described. Also described are processes for preparing N-substituted indenoisoquinoline compounds. Also described are methods for treating cancer in mammals using the described N-substituted indenoisoquinoline compounds or pharmaceutical formulations thereof.

IPC Classes  ?

  • C07D 221/18 - Ring systems of four or more rings
  • A61K 31/435 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom

31.

Scytovirin domain 1 related polypeptides

      
Application Number 11914833
Grant Number 08067530
Status In Force
Filing Date 2006-05-24
First Publication Date 2008-12-18
Grant Date 2011-11-29
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • O'Keefe, Barry R.
  • Xiong, Chang-Yun
  • Mcmahon, James B.
  • Byrd, Andrew

Abstract

A scytovirin domain 1 (SD1) polypeptide, a nucleic acid encoding the polypeptide, and related fusion proteins, conjugates, isolated cells, vectors, and antibodies, as well as a method of inhibiting a viral infection using the same.

IPC Classes  ?

  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • C12N 1/00 - Microorganisms, e.g. protozoaCompositions thereofProcesses of propagating, maintaining or preserving microorganisms or compositions thereofProcesses of preparing or isolating a composition containing a microorganismCulture media therefor
  • C12N 1/12 - Unicellular algaeCulture media therefor
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • A61K 38/00 - Medicinal preparations containing peptides
  • A01N 37/18 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N, e.g. carboxylic acid amides or imidesThio-analogues thereof

32.

Monoclonal antibodies to HIV-1 and methods of using same

      
Application Number 11630880
Grant Number 07993647
Status In Force
Filing Date 2005-06-22
First Publication Date 2008-11-27
Grant Date 2011-08-09
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Kopp, Jeffrey B.
  • Phillips, Terence M.
  • Schubert, Ulrich
  • Yewdell, John

Abstract

The present invention provides monoclonal antibodies to HIV-1 Vpr and hybridoma cell lines that produce the monoclonal antibodies to HIV-1 Vpr. Methods for use of such antibodies in the detection of HIV-1 infection are also provided.

IPC Classes  ?

  • A61K 39/42 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum viral
  • C12P 21/08 - Monoclonal antibodies
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

33.

Methods of using deacetylase inhibitors to promote cell differentiation and regeneration

      
Application Number 11800151
Grant Number 07795208
Status In Force
Filing Date 2007-05-04
First Publication Date 2008-10-09
Grant Date 2010-09-14
Owner
  • The Salk Institute for Biological Study (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Sartorelli, Vittorio
  • Puri, Pier Lorenzo

Abstract

A method of enhancing progenitor cell differentiation, including enhancing myogenesis, neurogenesis, and hematopoiesis, by contacting a progenitor cell with an effective amount of a deacetylase inhibitor (DI). The progenitor cell can be part of cell culture, such as a cell culture used for in vitro or in vivo analysis of progenitor cell differentiation, or can be part of an organism, such as a human or other mammal. Contacting the progenitor cell with a DI can lead to enhancement of expression of terminal cell-type specific genes in the progenitor cell, such as enhancing expression of muscle-specific genes in myoblasts. Administering a DI to a subject also can provide some prophylactic or therapeutic effect for inhibiting, preventing, or treating associated with a degeneration or loss of tissue. The DI can be administered to a subject as part of a pharmaceutical composition.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides
  • A61K 31/557 - Eicosanoids, e.g. leukotrienes
  • A61K 31/165 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide

34.

Venous filters

      
Application Number 10588863
Grant Number 07867245
Status In Force
Filing Date 2005-02-08
First Publication Date 2008-09-25
Grant Date 2011-01-11
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Neeman, Ziv
  • Wood, Bradford J.

Abstract

Venous filters having at least two struts (110) each having a connected end and a non-connected end, wherein each of the struts includes a strut portion and an anchor portion (116), and wherein the strut portion and the anchor portion are attached via an electrolytically active thread (221, 222); and a head (118) that connects the connected ends of the struts, wherein the strut portion can be separated from the anchor portion at least in part by the application of an electrical current. The invention also includes a venous filter having at least two struts, wherein each of the struts includes a temperature sensitive portion and an anchor portion; wherein the anchor portion is separated from the temperature sensitive portion at least in part by changing the temperature around at least the temperature sensitive portion. Also included is a venous filter having a web (650) of dissolvable material; and at least two anchors (618), wherein the at least two anchors are configured to retain the web within a mammalian blood vessel.

IPC Classes  ?

  • A61M 29/00 - Dilators with or without means for introducing media, e.g. remedies

35.

Desferrithiocin polyether analogues

      
Application Number 11973001
Grant Number 08278458
Status In Force
Filing Date 2007-10-04
First Publication Date 2008-09-04
Grant Date 2012-10-02
Owner
  • University of Florida Research Foundation, Inc. (USA)
  • University of Florida (USA)
  • The United States of America as Represented by the National Institutes of Health (NIH) (USA)
  • The United States of America as Represented by the Department of Health and Human Services (USA)
Inventor Bergeron, Jr., Raymond J.

Abstract

Compounds represented by structural formulas described herein, such as Structural Formula (I): or a pharmaceutically acceptable salt thereof are useful in treating conditions such as metal overload, oxidative stress, and neoplastic and preneoplastic conditions.

IPC Classes  ?

  • A61K 31/425 - Thiazoles
  • C07D 277/10 - Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

36.

ADP-ribosyl acceptor hydrolase 3 (ARH3) polypeptides and methods of use

      
Application Number 12047185
Grant Number 07670806
Status In Force
Filing Date 2008-03-12
First Publication Date 2008-08-28
Grant Date 2010-03-02
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Moss, Joel
  • Oka, Shunya
  • Kato, Jiro
  • Zhu, Jianfeng
  • Kasamatsu, Atsushi

Abstract

This disclosure provides methods for catalyzing the release of ADP-ribose from poly(ADP-ribose) or O-acetyl-ADP-ribose. Also provided are methods for modifying DNA repair or chromatin structure by introducing into the cell an agent that modifies the activity of an ARH3 polypeptide, or variant or fragment thereof. Further provided are methods for screening molecules involved in the poly(ADP-ribosyl)ation of proteins or O-acetyl-ADP-ribose content, and method for treating disorders by altering activity of an ARH3 protein.

IPC Classes  ?

  • C12P 19/00 - Preparation of compounds containing saccharide radicals
  • C12N 9/00 - Enzymes, e.g. ligases (6.)ProenzymesCompositions thereofProcesses for preparing, activating, inhibiting, separating, or purifying enzymes
  • C12N 1/20 - BacteriaCulture media therefor
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

37.

Nandrolone 17β-carbonates

      
Application Number 11815532
Grant Number 07820642
Status In Force
Filing Date 2006-01-24
First Publication Date 2008-07-10
Grant Date 2010-10-26
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Blye, Richard P.
  • Kim, Hyun K.

Abstract

Disclosed are compounds of the formula (I) 30 alkyl or halo, and the bond between C14 and C15 can be a single bond or double bond. Also disclosed are pharmaceutical compositions comprising such compounds and methods of use thereof. These compounds can find use in treating a number of diseases or conditions such as hypogonadism, osteoporosis, and anemia, in providing hormonal therapy and contraception, as an anabolic agent, and in suppressing the release of hormones such as the luteinizing hormone.

IPC Classes  ?

  • A61K 31/56 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids
  • C07J 1/00 - Normal steroids containing carbon, hydrogen, halogen, or oxygen, not substituted in position 17 beta by a carbon atom, e.g. oestrane, androstane

38.

Peptidomimetics that mimic a conformational-dependent neutralizing epitope of the human immunodeficiency virus (HIV) CCR5 coreceptor

      
Application Number 11578122
Grant Number 07700273
Status In Force
Filing Date 2005-04-11
First Publication Date 2008-07-03
Grant Date 2010-04-20
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Golding, Hana
  • Khurana, Surender

Abstract

The present invention relates, e.g., to an isolated peptide comprising a sequence of contiguous amino acids that is at least about 60% identical (e.g., at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98% or 100% identical) to the sequence E-W-Q-K-E-G-L-V-T-L-W-L (SEQ ID NO:1), or an active variant of an isolated peptide comprising SEQ ID NO:1. Neutralizing antibodies generated by, or specific for, such peptides are also described, in particular antibodies which are specific for the HIV co-receptor, CCR5, and which inhibit infection of a host cell by HIV. Neutralizing single strand and complete human monoclonal antibodies against CCR5 are described. Methods of using such peptides or antibodies, for inhibiting infection by HIV, are also described.

IPC Classes  ?

  • A61K 39/21 - Retroviridae, e.g. equine infectious anemia virus
  • C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
  • B01L 3/00 - Containers or dishes for laboratory use, e.g. laboratory glasswareDroppers

39.

Diagnostic tool for diagnosing benign versus malignant thyroid lesions

      
Application Number 11547995
Grant Number 07901881
Status In Force
Filing Date 2005-04-11
First Publication Date 2008-06-19
Grant Date 2011-03-08
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • The John Hopkins University (USA)
Inventor
  • Libutti, Steven K.
  • Mazzanti, Chiara
  • Zeiger, Martha
  • Umbricht, Christopher

Abstract

The present invention relates to the use of genes differentially expressed in benign thyroid lesions and malignant thyroid lesions for the diagnosis and staging of thyroid cancer.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

40.

Method of detecting cancer based on immune reaction to BORIS

      
Application Number 11575732
Grant Number 07785814
Status In Force
Filing Date 2005-09-21
First Publication Date 2008-04-24
Grant Date 2010-08-31
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Lobanenkov, Victor V.
  • Loukinov, Dmitri
  • Abdullaev, Ziedulla
  • Pack, Svetlana

Abstract

The invention provides a method of detecting a proliferative disease, such as a disease associated with the abnormal expression of BORIS, in a mammal comprising detecting antibodies to BORIS in a sample obtained from the mammal. The invention also provides BORIS polypeptides as well as compositions and kits comprising the BORIS polypeptides and methods of using the same. The invention further provides a method of inducing an immune response in a mammal using BORIS polypeptides.

IPC Classes  ?

  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer

41.

Wide-area fluorescence detection system for multi-photon microscopy

      
Application Number 11979600
Grant Number 07667210
Status In Force
Filing Date 2007-11-06
First Publication Date 2008-03-13
Grant Date 2010-02-23
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Balaban, Robert S.
  • Combs, Christian A.
  • Knutson, Jay R.

Abstract

A multi-photon microscope has an illumination source, an objective lens unit arranged in an optical path of the illumination source, a first light collection system arranged to collect a first portion of light emitted from a sample when the sample is illuminated by light from the illumination source, and a second light collection system arranged to collect a second portion of light emitted from the sample when the sample is illuminated by light from the illumination source. The first portion of light when collected by the first light collection system and the second portion of light when collected by the second light collection system, together provide a means of collecting as much light from as many angles as possible emanating from an emitting point source. This collection scheme has the potential to approach the total emission collection of light from an emitting point source depending on the optical properties of the sample being imaged.

IPC Classes  ?

  • G01J 1/58 - Photometry, e.g. photographic exposure meter using luminescence generated by light

42.

Adoptive immunotherapy with enhanced T lymphocyte survival

      
Application Number 11576621
Grant Number 07998736
Status In Force
Filing Date 2005-10-07
First Publication Date 2008-02-28
Grant Date 2011-08-16
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Morgan, Richard A.
  • Rosenberg, Steven A.
  • Hsu, Cary

Abstract

The invention provides for compositions, e.g., pharmaceutical compositions, comprising a T lymphocyte, or a population thereof, expressing at least one recombinant polynucleotide encoding a cytokine that enhances T lymphocyte survival during the contraction phase of an immune response. The invention further provides an isolated T lymphocyte, or population thereof, expressing at least one recombinant polynucleotide encoding the cytokine, wherein the polynucleotide comprises a non-native coding sequence encoding the cytokine. Also provided is the use of such compositions and T lymphocytes, or populations thereof, for the treatment or prevention of a medical condition e.g., cancer. A method of preparing the a T lymphocyte with enhanced T cell survival is further provided herein.

IPC Classes  ?

  • C12N 5/10 - Cells modified by introduction of foreign genetic material, e.g. virus-transformed cells
  • C12N 5/16 - Animal cells
  • C12N 5/0783 - T cellsNK cellsProgenitors of T or NK cells
  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy

43.

Use of CPG oligodeoxynucleotides to induce angiogenesis

      
Application Number 11839217
Grant Number 07935351
Status In Force
Filing Date 2007-08-15
First Publication Date 2008-01-31
Grant Date 2011-05-03
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • University of Tennessee Research Foundation (USA)
Inventor
  • Klinman, Dennis M.
  • Zheng, Mei
  • Rouse, Barry T.

Abstract

This disclosure provides a method of inducing production of vascular endothelial growth factor by a cell. The method includes contacting the cell with a CpG oligonucleotide, thereby inducing the production of vascular endothelial growth factor by the cell. The disclosure further provides a method inducing neovascularization in a tissue. This method includes comprising introducing a CpG oligodeoxynucleotide into an area of the tissue wherein the formation of new blood vessels is desired, thereby inducing neovascularization in the area of the tissue.

IPC Classes  ?

  • A61K 39/00 - Medicinal preparations containing antigens or antibodies
  • A61K 39/38 - Antigens from snakes
  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • A61K 47/00 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additivesTargeting or modifying agents chemically bound to the active ingredient
  • A01N 43/04 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atom with one hetero atom

44.

Estimation of the average propagator from magnetic resonance data

      
Application Number 11407096
Grant Number 07711171
Status In Force
Filing Date 2006-04-20
First Publication Date 2007-10-25
Grant Date 2010-05-04
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Basser, Peter J.
  • Pickalov, Valery

Abstract

An average propagator is estimated from diffusion-weighted magnetic resonance data. Diffusion-weighted signal attenuation data is determined from the diffusion-weighted magnetic resonance data. Estimated average propagator data is determined from the diffusion-weighted signal attenuation data based on at least one of a priori information of the diffusion-weighted signal attenuation data or a priori information of the average propagator.

IPC Classes  ?

  • G06K 9/00 - Methods or arrangements for reading or recognising printed or written characters or for recognising patterns, e.g. fingerprints

45.

Spectrally selective suppression with steady-state free precession

      
Application Number 11751479
Grant Number 07880466
Status In Force
Filing Date 2007-05-21
First Publication Date 2007-09-27
Grant Date 2011-02-01
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Derbyshire, John Andrew
  • Herzka, Daniel Alfredo
  • Mcveigh, Elliot R.

Abstract

A method for fat-suppressed imaging is disclosed. Such a method may include storing a first spectral component of an echo signal formed at TR/2 from a sample, suppressing a second spectral component of the echo signal at TR/2, re-exciting the stored spectral component after suppressing the second spectral component, and producing an image of the sample based on the re-excited stored spectral component.

IPC Classes  ?

  • G01V 3/00 - Electric or magnetic prospecting or detectingMeasuring magnetic field characteristics of the earth, e.g. declination or deviation

46.

Induction of tolerance by oral administration of factor VIII and treatment of hemophilia

      
Application Number 11734489
Grant Number 07867974
Status In Force
Filing Date 2007-04-12
First Publication Date 2007-08-02
Grant Date 2011-01-11
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • Virginia Tech Intellectual Properties, Inc. (USA)
Inventor
  • Alpan, Oral
  • Kamala, Tirumalai
  • Matzinger, Polly
  • Velander, William Hugold

Abstract

Disclosed herein is a simple method for the treatment of antigen-deficiency diseases, by orally administering to a subject a therapeutically effective amount of the deficient antigen, wherein the antigen is not present in a liposome. In one embodiment, the method increases hemostasis in a subject having hemophilia A or B, by orally administering to the hemophiliac a therapeutically effective amount of the appropriate clotting factor other than in a liposome, sufficient to induce oral tolerance and supply exogenous clotting factor to the subject.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides

47.

Methods of determining whether a pregnant woman is at risk of developing preeclampsia

      
Application Number 11346694
Grant Number 07790463
Status In Force
Filing Date 2006-02-02
First Publication Date 2007-08-02
Grant Date 2010-09-07
Owner
  • Yale University (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Mor, Gil G.
  • Neale, Donna
  • Romero, Roberto

Abstract

The present invention provides methods and compositions related to biomarker profiles for each trimester of pregnancy. The present invention also provides methods for identifying patients at risk of developing a complication of pregnancy, such as preeclampsia. In further embodiments, the present invention relates to methods for the diagnosis of patients with preeclampsia.

IPC Classes  ?

  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • C07K 1/00 - General processes for the preparation of peptides

48.

Method of DNA analysis using micro/nanochannel

      
Application Number 11633232
Grant Number 07960105
Status In Force
Filing Date 2006-11-29
First Publication Date 2007-07-12
Grant Date 2011-06-14
Owner
  • National Institutes of Health (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • U.S. Government NIH Division of Extramural Inventions and Technology Resources (USA)
Inventor
  • Schwartz, David C.
  • Jo, Kyubong
  • Dhingra, Dalia M.

Abstract

Methods are provided for tagging, characterizing and sorting double-stranded biomolecules while maintaining the integrity of the biomolecules.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12M 1/34 - Measuring or testing with condition measuring or sensing means, e.g. colony counters
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

49.

Chondropsin-class antitumor V-ATPase inhibitor compounds, compositions and methods of use thereof

      
Application Number 11674245
Grant Number 07521475
Status In Force
Filing Date 2007-02-13
First Publication Date 2007-06-21
Grant Date 2009-04-21
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Boyd, Michael R.
  • Gustafson, Kirk R.

Abstract

A composition comprising a substantially purified compound of the formula: in combination with at least one additional therapeutic agent, and methods of preventing or treating cancer and a condition treatable by the inhibition of vacuolar-type (H+)-ATPase.

IPC Classes  ?

  • A01N 43/16 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atom with one hetero atom six-membered rings with oxygen as the ring hetero atom
  • A61K 31/35 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom

50.

Particle image velocimetry system having an improved hollow-waveguide-based laser illumination system

      
Application Number 11589310
Grant Number 07787106
Status In Force
Filing Date 2006-10-30
First Publication Date 2007-05-24
Grant Date 2010-08-31
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Ilev, Ilko K.
  • Robinson, Ronald A.
  • Waynant, Ronald W.

Abstract

An illumination system for a particle image velocimetry system has an illumination source, a hollow tapered optical funnel arranged to receive illumination light from the illumination source, a hollow optical waveguide optically coupled to an output end of the hollow tapered optical funnel, and a beam shaping optical system optically coupled to an output end of the hollow optical waveguide. The illumination system is constructed to provide a light sheet to illuminate particles within a fluid under observation. A particle image velocimetry system has such an illumination system.

IPC Classes  ?

  • G01P 3/36 - Devices characterised by the use of optical means, e.g. using infrared, visible, or ultraviolet light

51.

PROPHYLAXIS AND TREATMENT OF ENTEROCOLITIS ASSOCIATED WITH ANTI-CTLA-4 ANTIBODY THERAPY

      
Application Number US2006043690
Publication Number 2007/056539
Status In Force
Filing Date 2006-11-08
Publication Date 2007-05-18
Owner
  • MEDAREX, INC. (USA)
  • UNITED STATES OF AMERICA as represented by THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (USA)
Inventor
  • Fischkoff, Steven
  • Lowy, Israel
  • Yang, James, Chung-Yin
  • Targan, Stephan, R.

Abstract

The present invention provides methods for reducing the incidence of adverse events related to immunotherapy. More specifically, the present invention provides methods for reducing the incidence of enterocolitis associated with anti- CTLA-4 antibody immunotherapy.

IPC Classes  ?

  • A01N 45/00 - Biocides, pest repellants or attractants, or plant growth regulators containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
  • A61K 31/56 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies

52.

TNF-ALPHA BLOCKER TREATMENT FOR ENTEROCOLITIS ASSOCIATED WITH IMMUNOSTIMULATORY THERAPEUTIC ANTIBODY THERAPY

      
Application Number US2006043691
Publication Number 2007/056540
Status In Force
Filing Date 2006-11-08
Publication Date 2007-05-18
Owner
  • MEDAREX, INC. (USA)
  • United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Fischkoff, Steven
  • Lowy, Israel
  • Yellin, Michael
  • Yang, James, Chung-Yin

Abstract

The present invention provides methods for treating adverse events related to immunotherapy. More specifically, the present invention provides methods for treating the enterocolitis associated with anti-CTLA-4 antibody immunotherapy.

IPC Classes  ?

  • A61K 38/16 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof
  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • C07K 14/00 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof
  • C07K 16/00 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies

53.

In situ assembling of protein microarrays

      
Application Number 11252735
Grant Number 08148302
Status In Force
Filing Date 2005-10-19
First Publication Date 2007-04-19
Grant Date 2012-04-03
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Chatterjee, Deb K
  • Sitaraman, Kalavathy
  • Hartley, James L
  • Baptista, Cassio
  • Munroe, David J

Abstract

The invention provides a microarray and methods for producing a protein microarray. The array comprises multiple nucleic acid molecules immobilized on a substrate, each comprising (i) a protein-binding domain and (ii) a nucleic acid sequence encoding a fusion protein comprising a polypeptide of interest and a DNA-binding protein that binds the protein-binding domain, and one or more fusion proteins produced from the multiple nucleic acid molecules. Each fusion protein is immobilized on the substrate via binding to a nucleic acid sequence comprising the protein-binding domain present on the nucleic acid molecule from which the fusion protein is produced or on the substrate. The invention also provides a method of analyzing protein interactions with, for example, other proteins, lipids and drugs.

IPC Classes  ?

  • C40B 40/08 - Libraries containing RNA or DNA which encodes proteins, e.g. gene libraries
  • C12N 15/63 - Introduction of foreign genetic material using vectorsVectorsUse of hosts thereforRegulation of expression

54.

1 sensitivity

      
Application Number 11147151
Grant Number 07787930
Status In Force
Filing Date 2005-06-06
First Publication Date 2006-11-09
Grant Date 2010-08-31
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • The Johns Hopkins University (USA)
Inventor
  • Nezafat, Reza
  • Ouwerkerk, Ronald
  • Stuber, Matthias

Abstract

2 prep sequence typically includes a first 90° pulse, an even number of adiabatic pulses, and a second 90° pulse. Adiabatic pulses can be selected based on function pairs, or can be defined numerically. A magnetic resonance imaging (MRI) system includes a library of adiabatic pulse waveforms, and is configured to select a waveform and apply an RF magnetic field based on the selected pulse waveform.

IPC Classes  ?

  • A61B 5/00 - Measuring for diagnostic purposes Identification of persons

55.

Inducible plasmid vector encoding TGF-β and use thereof

      
Application Number 10258109
Grant Number 07531352
Status In Force
Filing Date 2001-04-20
First Publication Date 2006-10-19
Grant Date 2009-05-12
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Strober, Warren
  • Nakamura, Kazuhiko
  • Kitani, Atsushi
  • Fuss, Jr., Ivan J.

Abstract

The present invention provides alternatives to traditional drug and surgical treatments for IBD. In particular, the present invention provides compositions and methods for the treatment of autoimmune diseases such as IBD in humans using TGF-β therapy. The compositions of the present invention provide vectors containing TGF-β under the control of an inducible promoter. In particularly preferred embodiments, the present invention provides regulated plasmid constructs capable of inducing TGF-β production. In preferred embodiments, the methods of the present invention utilize the vectors described for assaying the expression of a gene in a cell. In some preferred embodiments, the methods of the present invention utilize the administration of TGF-β containing vectors to treat IBD. In alternative preferred embodiments, the present invention provides methods and compositions for the induction of high-level interleukin (e.g., IL-10) production.

IPC Classes  ?

  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • C12N 5/02 - Propagation of single cells or cells in suspensionMaintenance thereofCulture media therefor

56.

System for monitoring exposure to impulse noise

      
Application Number 10564860
Grant Number 07401519
Status In Force
Filing Date 2004-07-13
First Publication Date 2006-10-05
Grant Date 2008-07-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor Kardous, Chucri A.

Abstract

In one embodiment, a system for monitoring exposure to impulse noise includes a sound-sensing device, such as a microphone or other type of pressure transducer, operable to sense impulse noise, and a storage module operable to store the waveform of the impulse noise sensed by the sound-sensing device. The sound-sensing device desirably is operable to sense impulses that are greater than 146 dB, such as impulses created by construction machinery and firearms. The system also can include a processor operable to calculate one or more noise parameters of the impulse noise from the waveform, and a user interface program operable to display said one or more noise parameters selected by a user.

IPC Classes  ?

  • G01H 17/00 - Measuring mechanical vibrations or ultrasonic, sonic or infrasonic waves, not provided for in the other groups of this subclass
  • H04R 29/00 - Monitoring arrangementsTesting arrangements
  • A61F 11/06 - Protective devices for the ears

57.

Methods for expression and purification of immunotoxins

      
Application Number 10566886
Grant Number 07892786
Status In Force
Filing Date 2004-08-02
First Publication Date 2006-09-28
Grant Date 2011-02-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Neville, David M.
  • Woo, Jung-Hee
  • Liu, Yuan-Yi

Abstract

Pichia pastoris in a growth medium comprising an enzymatic digest of protein and yeast extract and maintaining a dissolved oxygen concentration at 40% and above; and b) performing methanol induction with a limited methanol feed of 0.5-0.75 ml/min/IO L of initial volume during induction along with a continuous infusion of yeast extract at a temperature below 17.5° C., antifoaming agent supplied up to 0.07%, agitation reduced to 400 RPM, and the induction phase extended out to 163 h.

IPC Classes  ?

  • C12N 15/09 - Recombinant DNA-technology
  • C12N 15/10 - Processes for the isolation, preparation or purification of DNA or RNA
  • C12N 15/81 - Vectors or expression systems specially adapted for eukaryotic hosts for fungi for yeasts

58.

Internal control nucleic acid molecule for nucleic acid amplification systems

      
Application Number 11280474
Grant Number 07728123
Status In Force
Filing Date 2005-11-15
First Publication Date 2006-07-27
Grant Date 2010-06-01
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Vickery, Michael C. L.
  • Depaola, Angelo
  • Blackstone, George M.

Abstract

The invention provides an internal control nucleic acid molecule including at least one forward primer binding site, at least one reverse primer binding site, and at least one amplifiable region, wherein the forward primer binding site, the reverse primer binding site, and the amplifiable region are all randomly generated. The invention also provides a kit that includes at least one internal control nucleic acid molecule of the invention, at least one forward primer, configured to be complementary to the forward primer binding site of the internal control nucleic acid molecule, and at least one reverse primer, configured to be complementary to the reverse primer binding site of the internal control nucleic acid molecule. The invention also provides methods of using the internal control nucleic acid molecules and kits of the invention.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

59.

Wipes and methods for removal of metal contamination from surfaces

      
Application Number 11039178
Grant Number 07604997
Status In Force
Filing Date 2005-01-18
First Publication Date 2006-07-20
Grant Date 2009-10-20
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Esswein, Eric J.
  • Boeniger, Mark F.
  • Ashley, Kevin E.

Abstract

Wipes, methods and kits useful for testing and/or removal of metal from surfaces (such as, dermal surfaces) are disclosed. Exemplar wipes, including the combination of a three-dimensionally textured absorbent support, a cationic surfactant, and a weak acid, are disclosed. In some examples, the cationic surfactant is isostearamidopropyl morpholine lactate (ISML), and the weak acid is citric acid.

IPC Classes  ?

  • G01N 33/20 - Metals
  • G01N 21/25 - ColourSpectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands

60.

Recombinant vaccinia virus containing a chimeric gene having foreign DNA flanked by vaccinia regulatory DNA

      
Application Number 07987546
Grant Number 07045313
Status In Force
Filing Date 1992-12-07
First Publication Date 2006-05-16
Grant Date 2006-05-16
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Moss, Bernard
  • Mackett, Michael
  • Smith, Geoffrey

Abstract

Methods and compositions are provided for the use of vaccinia virus or other poxviruses as vectors for expression of foreign genes. Expression of foreign genes is obtained by combining vaccinia virus transcriptional regulatory sequence with uninterrupted foreign protein coding sequences in vitro to form a chimeric gene. The chimeric gene is flanked by DNA from a non-essential region of the vaccinia virus genome to provide sites for in vivo homologous recombination. These steps are facilitated by the construction of plasmids that contain multiple restriction endonuclease sites, next to the vaccinia transcriptional regulatory sequences, for insertion of any foreign protein coding sequence. Transfection procedures are used to introduce the DNA into cells where homologous recombination results in the insertion of the chimeric gene into a non-essential region of the vaccinia virus genome. Infectious vaccinia virus recombinants are distinguished or selected by expression of the foreign gene, loss of activity of a vaccinia virus gene, or by DNA—DNA hybridization. Expression of the foreign gene is obtained by infecting cells or animals with the recombinant vaccinia virus. Examples are provided to show expression of prokaryotic, RNA virus and other DNA virus genes in vaccinia recombinants.

IPC Classes  ?

  • C12P 21/06 - Preparation of peptides or proteins produced by the hydrolysis of a peptide bond, e.g. hydrolysate products

61.

Method of identifying active chromatin domains

      
Application Number 11087896
Grant Number 07527970
Status In Force
Filing Date 2005-03-23
First Publication Date 2006-04-20
Grant Date 2009-05-05
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor Zhao, Keji

Abstract

The invention provides a method of mapping DNA-protein interactions within a genome by fixing living cells to cross-link DNA and proteins, lysing the cells, and isolating chromatin by immunoprecipitation. DNA is purified and a SAGE protocol is performed on the purified DNA to produce GMAT-tag sequences, which are compared to a genomic sequence of the living cells to map DNA-protein interactions. The invention further provides a method of identifying an active chromatin domain and a method of identifying aberrant chromatin acetylation, wherein chromatin immunoprecipitation is performed using an antibody recognizing acetylated histone protein.

IPC Classes  ?

  • C12N 5/02 - Propagation of single cells or cells in suspensionMaintenance thereofCulture media therefor
  • C12N 5/06 -
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor

62.

Tryptophan as a functional replacement for ADP-ribose-arginine in recombinant proteins

      
Application Number 10517565
Grant Number 07541139
Status In Force
Filing Date 2003-06-27
First Publication Date 2006-04-06
Grant Date 2009-06-02
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • University of Massachusetts (USA)
Inventor
  • Moss, Joel
  • Stevens, Linda
  • Bourgeois, Christelle
  • Bortell, Rita

Abstract

A method is disclosed for producing a polypeptide with a modified activity or stability, by replacing an arginine residue capable of being ADP-ribosylated with a tryptophan or a phenylalanine. In one embodiment, compositions are provided that include polypeptides, such as alpha defensin, with arginine-to-tryptophan or arginine-to-phenylalanine substitutions, where the arginine residue is capable of being ADP-ribosylated. In another embodiment, methods are disclosed for modifying an immune response in a subject.

IPC Classes  ?

  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12P 1/00 - Preparation of compounds or compositions, not provided for in groups , by using microorganisms or enzymesGeneral processes for the preparation of compounds or compositions by using microorganisms or enzymes
  • C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions

63.

Method of treating inflammatory arthropathies with suppressors of CpG oligonucleotides

      
Application Number 10523273
Grant Number 07514415
Status In Force
Filing Date 2003-07-31
First Publication Date 2006-04-06
Grant Date 2009-04-07
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Klinman, Dennis
  • Zeuner, Rainald
  • Verthelyi, Daniela
  • Gursel, Ihsan
  • Gursel, Mayda

Abstract

The present disclosure relates to oligodeoxynucleotides that suppress an immune response. Methods are disclosed for preventing or treating inflammatory arthropathies by administering a therapeutically effective amount of a suppressive oligodeoxynucleotide.

IPC Classes  ?

  • A61K 31/70 - CarbohydratesSugarsDerivatives thereof

64.

Method for diagnosis and treatment of vascular disease

      
Application Number 10534626
Grant Number 07708977
Status In Force
Filing Date 2003-11-12
First Publication Date 2006-03-16
Grant Date 2010-05-04
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Finkel, Toren
  • Hill, Jonathan M.
  • Quyyumi, Arshed A.

Abstract

A method for diagnosing decreased vascular function is disclosed. The method includes assaying the number of endothelial progenitor cells. A method for detecting increased cardiovascular risk is also disclosed, as is a method for diagnosing atherosclerosis. In one example, the methods include assaying the number of endothelial progenitor cells. A method for treating a subject with decreased vascular function is disclosed. The method includes administering a therapeutically effective amount of endothelial progenitor cells to the subject. In one embodiment, the subject has atherosclerosis.

IPC Classes  ?

  • A61K 49/00 - Preparations for testing in vivo
  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy
  • A61K 35/12 - Materials from mammalsCompositions comprising non-specified tissues or cellsCompositions comprising non-embryonic stem cellsGenetically modified cells
  • A61K 35/14 - BloodArtificial blood
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor
  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • C12N 5/07 - Animal cells or tissues
  • A01N 1/02 - Preservation of living parts

65.

Synthesis of indenoisoquinolines

      
Application Number 11125723
Grant Number 07495100
Status In Force
Filing Date 2005-05-09
First Publication Date 2006-02-02
Grant Date 2009-02-24
Owner
  • Purdue Research Foundation (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Cushman, Mark S.
  • Morrell, Andrew E.
  • Pommier, Yves G.

Abstract

Indenoisoquinolines and dihydroindenoisoquinolines are described. In particular, such compounds possessing one or more electron withdrawing substituents are described. The in vitro anticancer activities of these molecules tested in the National Cancer Institute's screen of 55 cell lines is described. The compounds tested for topoisomerase I (top1) inhibition is described.

IPC Classes  ?

66.

Method of preventing infections from bioterrorism agents with immunostimulatory CpG oligonucleotides

      
Application Number 10533634
Grant Number 07758876
Status In Force
Filing Date 2003-10-31
First Publication Date 2006-01-26
Grant Date 2010-07-20
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Klinman, Dennis M.
  • Ivins, Bruce
  • Verthelyi, Daniela

Abstract

The present disclosure relates to a method of preventing or treating an infection caused by a bioterrorism agent, specifically to a method of increasing an immune response to a bioterrorism agent using an oligodeoxynucleotide including a CpG motif, and a method of enhancing the immunogenicity of a vaccine against a bioterrorism agent using an oligodeoxynucleotide including a CpG motif.

IPC Classes  ?

  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups

67.

p. perniciosus polypeptides and methods of use

      
Application Number 10527500
Grant Number 07741437
Status In Force
Filing Date 2003-09-18
First Publication Date 2006-01-05
Grant Date 2010-06-22
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • Merial Limited (USA)
Inventor
  • Valenzuela, Jesus G.
  • Ribiero, Jose M. C.
  • Kamhawi, Shaden
  • Belkaid, Yasmine
  • Fischer, Laurent
  • Audonnet, Jean-Christophe
  • Milward, Francis

Abstract

Leishmaniasis are disclosed.

IPC Classes  ?

  • C07K 14/00 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof

68.

Plasmids and phages for homologous recombination and methods of use

      
Application Number 11134795
Grant Number 07674621
Status In Force
Filing Date 2005-05-20
First Publication Date 2005-12-08
Grant Date 2010-03-09
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Court, Donald L.
  • Datta, Simanti
  • Costantino, Nina

Abstract

Salmonella, Pseudomonas, Cyanobacteria, Spirochaetes. These plasmids and phages can be isolated in vitro and can be used to transform bacterial cells, such as gram negative bacteria.

IPC Classes  ?

  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12N 15/63 - Introduction of foreign genetic material using vectorsVectorsUse of hosts thereforRegulation of expression
  • C12N 15/70 - Vectors or expression systems specially adapted for E. coli

69.

Method and apparatus for countercurrent chromatography

      
Application Number 10509697
Grant Number 07892847
Status In Force
Filing Date 2003-03-25
First Publication Date 2005-11-03
Grant Date 2011-02-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor Ito, Yoichiro

Abstract

2) by a connecting channel (72). Septa may be provided between the plates to connect the spiral channels of one plate to the spiral channels of the next plate.

IPC Classes  ?

  • B01D 15/08 - Selective adsorption, e.g. chromatography
  • B07B 7/00 - Selective separation of solid materials carried by, or dispersed in, gas currents

70.

Antibodies, including Fv molecules, and immunoconjugates having high binding affinity for mesothelin and methods for their use

      
Application Number 10973718
Grant Number 07368110
Status In Force
Filing Date 2004-10-25
First Publication Date 2005-09-29
Grant Date 2008-05-06
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Pastan, Ira H.
  • Chowdhury, Partha S.

Abstract

Mesothelin ins a differentiation antigen present on the surface of ovarian cancers, mesotheliomas and several other types of human cancers. Because among normal tissues, mesothelin is only present on mesothelial cells, it represents a good target for antibody mediated delivery of cytotoxic agents. The present invention is directed to anti-mesothelin antibodies, including Fv molecules with particularly high affinity for mesothelin, and immunoconjugates employing them. Also described are diagnostic and therapeutic methods using the antibodies. The anti-mesothelin antibodies are well-suited for the diagnosis and treatment of cancers of the ovary, stomach, squamous cells, mesotheliomas and other malignant cells expressing mesothelin.

IPC Classes  ?

  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum

71.

Brother of the regulator of imprinted sites (BORIS)

      
Application Number 10505377
Grant Number 07375206
Status In Force
Filing Date 2003-02-21
First Publication Date 2005-08-18
Grant Date 2008-05-20
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Lobanenkov, Victor V.
  • Loukinov, Dmitri I.
  • Morse, Iii, Herbert C.

Abstract

An isolated or purified nucleic acid molecule consisting essentially of a nucleotide sequence encoding a human or a non-human BORIS, or a fragment of either of the foregoing; an isolated or purified nucleic acid molecule consisting essentially of a nucleotide sequence that is complementary to a nucleotide sequence encoding a human or a non-human BORIS, or a fragment of either of the foregoing; a vector comprising such an isolated or purified nucleic acid molecule; a cell comprising such a vector; an isolated or purified polypeptide molecule consisting essentially of an amino acid sequence encoding a human or a non-human BORIS, or a fragment of either of the foregoing; a cell line that produces a monoclonal antibody that is specific for an aforementioned isolated or purified polypeptide molecule; and the monoclonal antibody produced by the cell line; methods of diagnosing a cancer or a predisposition to a cancer in a male or female mammal; a method of prognosticating a cancer in a mammal; a method of assessing the effectiveness of treatment of a cancer in a mammal; a method of treating a mammal prophylactically or therapeutically for a cancer, and a composition comprising a carrier and an inhibitor of BORIS.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

72.

Methods for separation and detection of ketosteroids and other carbonyl-containing compounds

      
Application Number 10511409
Grant Number 07807472
Status In Force
Filing Date 2003-04-15
First Publication Date 2005-08-18
Grant Date 2010-10-05
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Xu, Xia
  • Ziegler, Regina G.
  • Waterhouse, David J.
  • Saavedra, Joseph E.
  • Keefer, Larry K.

Abstract

Methods for enhancing detection by mass spectroscopy (MS) and/or chromatographic separability of carbonyl-containing compounds such as steroids are disclosed. Reaction of a carbonyl compound with a sulfonhydrazide compound provides a sulfonhydrazone with enhanced ionization efficiency during the electrospray ionization process. In a particularly disclosed embodiment, derivatization of catechol estrogens with p-toluenesulfonhydrazide enhances both detection by atmospheric pressure ionization-MS (API-MS), such as electron spray ionization-MS (ESI-MS) and separation by liquid chromatography (such as HPLC) under reverse phase conditions. In yet other embodiments, the sulfonhydrazone is further reacted with a sulfonyl halide under alkaline conditions to derivatize hydroxyl groups in the compound. Prior formation of the sulfonhydrazide derivative protects the carbonyl bond of the compound during subsequent alkaline reaction with the sulfonyl halide.

IPC Classes  ?

  • G01N 33/00 - Investigating or analysing materials by specific methods not covered by groups
  • G01N 1/00 - SamplingPreparing specimens for investigation

73.

Methods for diagnosing lymphoma types

      
Application Number 10934930
Grant Number 07711492
Status In Force
Filing Date 2004-09-03
First Publication Date 2005-07-28
Grant Date 2010-05-04
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Staudt, Louis M.
  • Wright, George
  • Dave, Sandeep
  • Tan, Bruce

Abstract

Gene expression data provides a basis for more accurate identification and diagnosis of lymphoproliferative disorders. In addition, gene expression data can be used to develop more accurate predictors of survival. The present invention discloses methods for identifying, diagnosing, and predicting survival in a lymphoma or lymphoproliferative disorder on the basis of gene expression patterns. The invention discloses a novel microarray, the Lymph Dx microarray, for obtaining gene expression data from a lymphoma sample. The invention also discloses a variety of methods for utilizing lymphoma gene expression data to determine the identity of a particular lymphoma and to predict survival in a subject diagnosed with a particular lymphoma. This information will be useful in developing the therapeutic approach to be used with a particular subject.

IPC Classes  ?

  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12N 15/11 - DNA or RNA fragmentsModified forms thereof

74.

Chimeric molecule for the treatment of th2-like cytokine mediated disorders

      
Application Number 10497804
Grant Number 07541040
Status In Force
Filing Date 2005-02-10
First Publication Date 2005-06-30
Grant Date 2009-06-02
Owner
  • The United States of America as represented by the Department of Health and Human Serivces (USA)
  • The Regents of the University of Michigan, Office of Technology Transfer (USA)
Inventor
  • Puri, Raj K.
  • Hogaboam, Cory M.
  • Jakubzick, Claudia
  • Kunkel, Steven L.

Abstract

The invention provides uses and methods for alleviating respiratory tract symptoms of allergy, asthma, and of viral, bacterial, fungal and parasitic infections by shifting inappropriate TH2 responses to TH1 responses by administering IL-13 receptor-targeted immunotoxins to the respiratory tract.

IPC Classes  ?

75.

Methods and compositions for detecting dihydropyrimidine dehydrogenase splicing mutations

      
Application Number 10911237
Grant Number 07402387
Status In Force
Filing Date 2004-08-03
First Publication Date 2005-06-23
Grant Date 2008-07-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Gonzalez, Frank J.
  • Fernandez-Salguero, Pedro

Abstract

The present invention provides compositions, methods, and kits for the detection of genetic polymorphisms or mutations of the dihydropyrimidine dehydrogenase deficiency (DPDD). The polymorphisms or mutations generally occur in the dihydropyrimidine dehydrogenase (DPD) gene in chromosome 1. Also provided are mutant forms of DPD.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • C12N 9/02 - Oxidoreductases (1.), e.g. luciferase
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/32 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving oxidoreductase involving dehydrogenase
  • C07H 21/00 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
  • C07K 14/00 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof

76.

Determination of feature boundaries in a digital representation of an anatomical structure

      
Application Number 10779210
Grant Number 07454045
Status In Force
Filing Date 2004-02-13
First Publication Date 2005-04-14
Grant Date 2008-11-18
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Yao, Jianhua
  • Summers, Ronald M.

Abstract

A virtual anatomical structure can be analyzed to determine enclosing three-dimensional boundaries of features therein. Various techniques can be used to determine tissue types in the virtual anatomical structure. For example, tissue types can be determined via an iso-boundary between lumen and air in the virtual anatomical structure and a fuzzy clustering approach. Based on the tissue type determination, a deformable model approach can be used to determine an enclosing three-dimensional boundary of a feature in the virtual anatomical structure. The enclosing three-dimensional boundary can be used to determine characteristics of the feature and classify it as of interest or not of interest.

IPC Classes  ?

  • G06K 9/00 - Methods or arrangements for reading or recognising printed or written characters or for recognising patterns, e.g. fingerprints

77.

Host cells deficient for mismatch repair and their use in methods for inducing homologous recombination using single-stranded nucleic acids

      
Application Number 10841125
Grant Number 07521242
Status In Force
Filing Date 2004-05-07
First Publication Date 2005-04-14
Grant Date 2009-04-21
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Court, Donald L.
  • Li, Xin-Tian
  • Huang, Jian-Dong
  • Costantino, Nina
  • Liu, Depei

Abstract

Methods are disclosed herein for inducing homologous recombination in a host cell comprising a target nucleic acid, using a single-stranded nucleic acid molecule. The single-stranded nucleic acid molecule has a sufficient number of nucleotides homologous to the target nucleic acid to enable homologous recombination with the target nucleic acid. The host cell includes a de-repressible promoter operably linked to a nucleic acid encoding a single-stranded binding protein and is deficient for mismatch repair. Isolated host cells of use in this method are also disclosed.

IPC Classes  ?

  • C12N 15/87 - Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
  • C12N 15/90 - Stable introduction of foreign DNA into chromosome
  • C12N 1/21 - BacteriaCulture media therefor modified by introduction of foreign genetic material

78.

Pattern recognition of whole cell mass spectra

      
Application Number 10863745
Grant Number 07684934
Status In Force
Filing Date 2004-06-07
First Publication Date 2005-03-24
Grant Date 2010-03-23
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Shvartsburg, Alexandre
  • Wilkes, Jon G.
  • Chiarelli, Paul
  • Holland, Ricky D.
  • Buzatu, Dan A.
  • Beaudoin, Michael A.

Abstract

A method for reproducibly analyzing mass spectra from different sample sources is provided. The method deconvolutes the complex spectra by collapsing multiple peaks of different molecular mass that originate from the same molecular fragment into a single peak. The differences in molecular mass are apparent differences caused by different charge states of the fragment and/or different metal ion adducts and/or reactant products of one or more of the charge states. The deconvoluted spectrum is compared to a library of mass spectra acquired from samples of known identity to unambiguously determine the identity of one or more components of the sample undergoing analysis.

IPC Classes  ?

  • G06F 19/00 - Digital computing or data processing equipment or methods, specially adapted for specific applications (specially adapted for specific functions G06F 17/00;data processing systems or methods specially adapted for administrative, commercial, financial, managerial, supervisory or forecasting purposes G06Q;healthcare informatics G16H)

79.

Human derived monocyte attracting purified protein product useful in a method of treating infection and neoplasms in a human body, and the cloning of full length cDNA thereof

      
Application Number 07330446
Grant Number 06869924
Status In Force
Filing Date 1989-03-30
First Publication Date 2005-03-22
Grant Date 2005-03-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Yoshimura, Teizo
  • Robinson, Elizabeth A.
  • Appella, Ettore
  • Leonard, Edward J.

Abstract

Pure peptide products, derived from either human glioma cell line U-105MG or human peripheral blood mononuclear leukocytes are provided; the products have a molecular mass of about 8,400 daltons, and the products exhibit optimal monocyte chemotactic activity at a concentration of 1 nM. The cloning of full length cDNA for the peptide products is also provided, as well as recombinant methods for the production of monocyte chemoattractant products. Methods of treating infection and neoplasms in a human body with such peptides and monocyte chemoattractant products are additionally provided, as well as pharmaceutical compositions for the same.

IPC Classes  ?

  • C07K 14/00 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof

80.

Thermolabile hydroxyl protecting groups and methods of use

      
Application Number 10497416
Grant Number 07355037
Status In Force
Filing Date 2002-12-03
First Publication Date 2005-01-27
Grant Date 2008-04-08
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Beaucage, Serge L.
  • Grajkowski, Andrzej
  • Wilk, Andrzej

Abstract

Provided is a hydroxyl-protected alcohol of the formula R—O—Pg, wherein Pg is a protecting group of the formula: 4a, a, b, c, d, e and f are defined herein and R is a nucleosidyl group, an oligonucleotidyl group with 2 to about 300 nucleosides, or an oligomer with 2 to about 300 nucleosides. Also provided is a deprotection method, which includes heating the hydroxyl-protected alcohol at a temperature effective to cleave thermally the hydroxyl-protecting group therefrom.

IPC Classes  ?

  • C07H 21/00 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids

81.

Development of a preventive vaccine for filovirus infection in primates

      
Application Number 10491121
Grant Number 07635688
Status In Force
Filing Date 2004-08-23
First Publication Date 2004-12-23
Grant Date 2009-12-22
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Nabel, Gary J.
  • Yang, Zhi-Yong
  • Sullivan, Nancy
  • Sanchez, Anthony

Abstract

The present invention relates generally to viral vaccines and, more particularly, to filovirus vaccines and methods of eliciting an immune response against a filovirus or disease caused by infection with filovirus.

IPC Classes  ?

  • A61K 31/70 - CarbohydratesSugarsDerivatives thereof
  • A61K 49/00 - Preparations for testing in vivo
  • A01N 65/00 - Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
  • A61K 48/00 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseasesGene therapy
  • C12N 5/00 - Undifferentiated human, animal or plant cells, e.g. cell linesTissuesCultivation or maintenance thereofCulture media therefor
  • C12N 15/00 - Mutation or genetic engineeringDNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purificationUse of hosts therefor
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical

82.

Suppressors of CpG oligonucleotides and methods of use

      
Application Number 10489839
Grant Number 07514414
Status In Force
Filing Date 2004-03-16
First Publication Date 2004-12-09
Grant Date 2009-04-07
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Klinman, Dennis M.
  • Zeuner, Rainald
  • Gursel, Mayda
  • Gursel, Ihsan
  • Verthelyi, Daniela

Abstract

The present disclosure relates to oligodeoxynucleotides that suppress an immune response. Methods are disclosed for preventing or treating an immune-mediated disorder, such as, but not limited to, an autoimmune disease, by administering a therapeutically effective amount of a suppressive oligodeoxynucleotide. Also disclosed are methods of suppressing an immune response in a subject by administering a therapeutically effective amount of a suppressive oligodeoxynucleotide.

IPC Classes  ?

  • A61K 31/70 - CarbohydratesSugarsDerivatives thereof

83.

GLP-1 exendin-4 peptide analogs and uses thereof

      
Application Number 10485140
Grant Number 07576050
Status In Force
Filing Date 2004-04-01
First Publication Date 2004-12-02
Grant Date 2009-08-18
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Greig, Nigel
  • Egan, Josephine
  • Doyle, Maire
  • Holloway, Harold
  • Perry, Tracy Ann

Abstract

The invention relates to novel polypeptide analogues of GLP-1 and exendin-4. The polypeptide, in a preferred embodiment, is insulinotropic and long-acting. Preferably, the polypeptide's insulinotropic effect is comparable to or exceeds the effect of an equimolar amount of GLP-1 or exendin-4. The invention also relates to a method of treating a subject with diabetes, comprising administering to the subject the polypeptide of the invention in an amount that has an insulinotropic effect. The invention also relates to methods of using GLP-1, exendin-4, and polypeptide analogues thereof for neuroprotective and neurotrophic effects.

IPC Classes  ?

84.

Recovery of recombinant human parainfluenza virus type 2 (HPIV2) from cDNA and use of recombinant HPIV2 in immunogenic compositions and as vectors to elicit immune responses against PIV and other human pathogens

      
Application Number 10667141
Grant Number 07820181
Status In Force
Filing Date 2003-09-18
First Publication Date 2004-10-14
Grant Date 2010-10-26
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Skiadopoulos, Mario H.
  • Murphy, Brian R.
  • Collins, Peter L.

Abstract

Recombinant human parainfluenza virus type 2 (HPIV2) viruses and related immunogenic compositions and methods are provided. The recombinant HPIV2 viruses, including HPIV2 chimeric and chimeric vector viruses, provided according to the invention are infectious and attenuated in permissive mammalian subjects, including humans, and are useful in immunogenic compositions for eliciting an immune responses against one or more PIVs, against one or more non-PIV pathogens, or against a PIV and a non-PIV pathogen. Also provided are isolated polynucleotide molecules and vectors incorporating a recombinant HPIV2 genome or antigenome.

IPC Classes  ?

  • A61K 39/155 - Paramyxoviridae, e.g. parainfluenza virus

85.

Agents useful for reducing amyloid precursor protein and treating demantia and methods of use thereof

      
Application Number 10415765
Grant Number 07153882
Status In Force
Filing Date 2004-02-06
First Publication Date 2004-07-15
Grant Date 2006-12-26
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • The National Institutes of Health and Axonyx, Inc. (USA)
Inventor
  • Greig, Nigel H.
  • Shaw, Karen T. Y.
  • Yu, Qiang-Sheng
  • Holloway, Harold W.
  • Sencrant, Timothy T.
  • Utsuki, Tada
  • Ingram, Donald
  • Brossi, Arnold
  • Giordano, Anthony
  • Powers, Gordon
  • Davidson, Diane
  • Sturgess, Michael

Abstract

The present invention provides compounds and methods of administering compounds to a subject that can reduce βAPP production and that is not toxic in a wide range of dosages. The present invention also provides non-carbamate compounds and methods of administering such compounds to a subject that can reduce βAPP production and that is not tocix in a wide range of dosages. It has been discovered that either the racemic or enantiomerically pure non-carbamate compounds can be used to decrease βAPP production.

IPC Classes  ?

  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • C07D 487/02 - Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups in which the condensed system contains two hetero rings
  • C07D 491/02 - Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups , , or in which the condensed system contains two hetero rings

86.

Reduction of the nonspecific animal toxicity of immunotoxins by mutating the framework regions of the Fv to lower the isoelectric point

      
Application Number 10416129
Grant Number 07521054
Status In Force
Filing Date 2003-12-18
First Publication Date 2004-05-13
Grant Date 2009-04-21
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Pastan, Ira H.
  • Onda, Masanori
  • Nagata, Satoshi
  • Tsutsumi, Yasuo
  • Vincent, James J.
  • Kreitman, Robert J.
  • Vasmatzis, George
  • Lee, Byungkook

Abstract

The invention provides recombinant immunotoxins that have been modified from a parental immunotoxin to lower liver toxicity. The immunotoxins are created by specifically mutating charged residues in the framework regions of the heavy chain, the light chain, or both, of the antibody portion or antigen-binding fragment thereof of the parental immunotoxin to reduce the pI of the antibody or fragment. In preferred forms, the antibody portion of the parental is an anti-Tac, anti-mesothelin, or anti-LewisY antigen antibody or antigen-binding fragment, and in particularly preferred forms the antibody portion is an M16 dsFv, a St6 dsFv or a Mt9 dsFv, or a sequence that has at least 90% sequence identity to one of these molecules but retain the particular mutations that lower pI without affecting antibody activity. The invention further provides nucleic acids encoding the recombinant immunotoxins of the invention, expression cassettes comprising the nucleic acids, and host cells comprising the expression cassettes. The invention also provides a method for killing a cell comprising an antigen on the surface of the cell, the method comprising contacting the cell with a recombinant immunotoxin of the invention that has an antibody or antigen-binding fragment thereof that binds specifically to the antigen on the surface of the cell, and uses of immunotoxins of the invention for the manufacture of medicaments.

IPC Classes  ?

  • A61K 47/48 - Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants

87.

Bacillus anthracis protective antigen for use in vaccines

      
Application Number 10290712
Grant Number 07763451
Status In Force
Filing Date 2002-11-08
First Publication Date 2004-04-22
Grant Date 2010-07-27
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Shiloach, Joseph
  • Leppla, Stephen H.
  • Ramirez, Delia M.
  • Schneerson, Rachel
  • Robbins, John B.
  • Hsu, S. Dana
  • Rosovitz, Mary Jo

Abstract

B. anthracis, such as inhalation anthrax, cutaneous anthrax and gastrointestinal anthrax.

IPC Classes  ?

  • C12N 1/00 - Microorganisms, e.g. protozoaCompositions thereofProcesses of propagating, maintaining or preserving microorganisms or compositions thereofProcesses of preparing or isolating a composition containing a microorganismCulture media therefor
  • C12N 1/20 - BacteriaCulture media therefor
  • C12P 1/00 - Preparation of compounds or compositions, not provided for in groups , by using microorganisms or enzymesGeneral processes for the preparation of compounds or compositions by using microorganisms or enzymes
  • A61K 39/38 - Antigens from snakes
  • A61K 39/02 - Bacterial antigens
  • A61K 39/07 - Bacillus

88.

Coil for magnetic stimulation

      
Application Number 10399559
Grant Number 07407478
Status In Force
Filing Date 2003-10-09
First Publication Date 2004-04-22
Grant Date 2008-08-05
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Zangen, Abraham
  • Wise, Roy A.
  • Hallett, Mark
  • Miranda, Pedro Cavaleiro
  • Roth, Yiftach

Abstract

A magnetic stimulator, which may be used as a transcranial magnetic stimulation (TMS) device, and a method for its use are disclosed. The stimulator comprises a frame and an electrically conductive coil having a partially toroidal or ovate base and an outwardly projecting extension portion. The frame may be a flexible or malleable material and may be non-conductive. The electrically conductive coil may comprise one or more windings of electrically conductive material (such as a wire) coupled to the frame. The coil is electrically connected to a power supply. The device may be placed adjacent to or in contact with the body of a subject, such as on the head of a subject. The device may be used on humans for treating certain physiological conditions, such as cardiovascular or neurophysiological conditions, or for studying the physiology of the body. This device is useful in studying or treating neurophysiological conditions associated with the deep regions of the brain, such as drug addiction and depression.

IPC Classes  ?

  • A61N 1/00 - ElectrotherapyCircuits therefor

89.

SFRP and peptide motifs that interact with SFRP and methods of their use

      
Application Number 10466136
Grant Number 07488710
Status In Force
Filing Date 2003-07-10
First Publication Date 2004-04-22
Grant Date 2009-02-10
Owner
  • The United States of America as represented by the Department of Health and Human Services (USA)
  • St. Vincent's Institute of Medical Research (Australia)
Inventor
  • Rubin, Jeffrey S.
  • Üren, Aykut
  • Gillespie, Matthew Todd
  • Horwood, Nicole Joy

Abstract

This disclosure relates to a peptide motif and proteins containing the motif that are capable of binding to secreted Frizzled-related protein family members. Accordingly, the disclosure also includes methods of regulating the interaction of sFRP-1 with proteins containing the motif.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides

90.

Versatile reagent for detecting murine leukemia viruses

      
Application Number 08046352
Grant Number 06709811
Status In Force
Filing Date 1993-04-08
First Publication Date 2004-03-23
Grant Date 2004-03-23
Owner The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Evans, Leonard H
  • Britt, William J

Abstract

A method for detecting broad spectrum of murine leukemia viruses belonging to any or all of the ecotropic, xenotropic, polytropic and amphotropic groups, has been described. The method utilizes a monoclonal antibody designated 83A25 which identifies almost all classes or groups of the murine leukemia virus with only a few exceptions.

IPC Classes  ?

  • C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
  • C12N 5/20 - Murine cells, e.g. mouse cells one of the fusion partners being a B lymphocyte
  • C07K 16/10 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses

91.

Modification of the normalized difference method for real-time optical tomography

      
Application Number 10408511
Grant Number 07616984
Status In Force
Filing Date 2003-04-07
First Publication Date 2004-01-15
Grant Date 2009-11-10
Owner
  • National Institutes of Health (NIH) (USA)
  • The United States of America as represented by the Department of Health and Human Services (USA)
Inventor
  • Barbour, Randall L.
  • Pei, Yaling

Abstract

Computation-saving techniques and stability-adding techniques provide for fast, accurate reconstructions of a time series of images involving large-scale 3D problems, such as real-time image recovery in an optical tomography imaging system. A system equation for a target medium (116) such as tissue is solved using a Normalized Difference Method (NDM) (250). Because of the inherent stability of the NDM solutions, a weight matrix (W) of the system equation can be provided for a given point in a time series (220), then reused without recalculation at subsequent points. Further savings are achieved by decomposing W using singular value decomposition or direct matrix decomposition, transforming it to reduce its dimensions, and/or scaling it to achieve a more stable numerical solution. Values of measured energy (112) emerging from the target medium are back-substituted into the system equation for the different points to obtain the target medium properties.

IPC Classes  ?

  • A61B 6/00 - Apparatus or devices for radiation diagnosisApparatus or devices for radiation diagnosis combined with radiation therapy equipment