Ikaria, Inc.

United States of America

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2024 September 1
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IPC Class
A61P 39/00 - General protective or antinoxious agents 5
A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis 4
C12P 21/02 - Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione 4
A61K 33/04 - Sulfur, selenium or telluriumCompounds thereof 3
C07B 59/00 - Introduction of isotopes of elements into organic compounds 3
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NICE Class
05 - Pharmaceutical, veterinary and sanitary products 1
10 - Medical apparatus and instruments 1
42 - Scientific, technological and industrial services, research and design 1
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Registered / In Force 11

1.

FUNTIONALLY MODIFIED POLYPEPTIDES AND RADIOBIOSYNTHESIS

      
Application Number 18439838
Status Pending
Filing Date 2024-02-13
First Publication Date 2024-09-05
Owner IKARIA INC. (USA)
Inventor Dimagno, Stephen

Abstract

Provided herein are compositions and methods for generating polypeptides using non-natural amino acids (nnAAs) and genetic machinery, wherein the modified polypeptides, such as therapeutic polypeptides, bind to albumin, such as serum albumin. Methods of substituting a non-natural amino acid in a first polypeptide to obtain a modified polypeptide, the nnAA in some instances comprising an albumin targeting group, are disclosed, as are methods for making populations of such modified polypeptides. A therapeutic polypeptide, interleukin-1 receptor antagonist (IL-1RA) is exemplified using the disclosed methods.

IPC Classes  ?

  • C12P 21/02 - Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
  • C07B 59/00 - Introduction of isotopes of elements into organic compounds
  • C07C 233/51 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
  • C07C 327/42 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
  • C07C 327/44 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
  • C07K 14/54 - Interleukins [IL]
  • C07K 14/545 - IL-1
  • C12N 9/00 - Enzymes, e.g. ligases (6.)ProenzymesCompositions thereofProcesses for preparing, activating, inhibiting, separating, or purifying enzymes

2.

Functionally modified polypeptides and radiobiosynthesis

      
Application Number 17540316
Grant Number 11939617
Status In Force
Filing Date 2021-12-02
First Publication Date 2023-10-19
Grant Date 2024-03-26
Owner Ikaria Inc. (USA)
Inventor Dimagno, Stephen

Abstract

Provided herein are compositions and methods for generating polypeptides using non-natural amino acids (nnAAs) and genetic machinery, wherein the modified polypeptides, such as therapeutic polypeptides, bind to albumin, such as serum albumin. Methods of substituting a non-natural amino acid in a first polypeptide to obtain a modified polypeptide, the nnAA in some instances comprising an albumin targeting group, are disclosed, as are methods for making populations of such modified polypeptides. A therapeutic polypeptide, interleukin-1 receptor antagonist (IL-1RA) is exemplified using the disclosed methods.

IPC Classes  ?

  • C12P 21/02 - Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
  • C07B 59/00 - Introduction of isotopes of elements into organic compounds
  • C07C 233/51 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
  • C07C 327/42 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
  • C07C 327/44 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
  • C07K 14/54 - Interleukins [IL]
  • C07K 14/545 - IL-1
  • C12N 9/00 - Enzymes, e.g. ligases (6.)ProenzymesCompositions thereofProcesses for preparing, activating, inhibiting, separating, or purifying enzymes

3.

Functionally modified polypeptides and radiobiosynthesis

      
Application Number 15695831
Grant Number 11214820
Status In Force
Filing Date 2017-09-05
First Publication Date 2018-03-08
Grant Date 2022-01-04
Owner Ikaria Inc. (USA)
Inventor Dimagno, Stephen

Abstract

Provided herein are compositions and methods for generating polypeptides using non-natural amino acids (nnAAs) and genetic machinery, wherein the modified polypeptides, such as therapeutic polypeptides, bind to albumin, such as serum albumin. Methods of substituting a non-natural amino acid in a first polypeptide to obtain a modified polypeptide, the nnAA in some instances comprising an albumin targeting group, are disclosed, as are methods for making populations of such modified polypeptides. A therapeutic polypeptide, interleukin-1 receptor antagonist (IL-1RA) is exemplified using the disclosed methods.

IPC Classes  ?

  • C12P 21/02 - Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
  • C07C 327/44 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
  • C07C 233/51 - Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
  • C07K 14/545 - IL-1
  • C07B 59/00 - Introduction of isotopes of elements into organic compounds
  • C07C 327/42 - Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
  • C07K 14/54 - Interleukins [IL]
  • C12N 9/00 - Enzymes, e.g. ligases (6.)ProenzymesCompositions thereofProcesses for preparing, activating, inhibiting, separating, or purifying enzymes

4.

FUNCTIONALLY MODIFIED POLYPEPTIDES AND RADIOBIOSYNTHESIS

      
Application Number US2017050082
Publication Number 2018/045376
Status In Force
Filing Date 2017-09-05
Publication Date 2018-03-08
Owner IKARIA INC. (USA)
Inventor Dimagno, Stephen

Abstract

Provided herein are compositions and methods for generating polypeptides using non-natural amino acids (nnAAs) and genetic machinery, wherein the modified polypeptides, such as therapeutic polypeptides, bind to albumin, such as serum albumin. Methods of substituting a non-natural amino acid in a first polypeptide to obtain a modified polypeptide, the nnAA in some instances comprising an albumin targeting group, are disclosed, as are methods for making populations of such modified polypeptides. A therapeutic polypeptide, interleukin-1 receptor antagonist (IL-1RA) is exemplified using the disclosed methods.

IPC Classes  ?

  • C12N 15/09 - Recombinant DNA-technology
  • C12N 15/67 - General methods for enhancing the expression
  • C12P 13/00 - Preparation of nitrogen-containing organic compounds
  • C12P 21/02 - Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione

5.

COMPOSITIONS, METHODS AND ARTICLES CONCERNING PHARMACEUTICAL NITRIC OXIDE AND CONTROLLED PATIENT DELIVERY SYSTEMS THEREOF

      
Application Number US2011051106
Publication Number 2012/034089
Status In Force
Filing Date 2011-09-09
Publication Date 2012-03-15
Owner IKARIA, INC. (USA)
Inventor
  • Montgomery, Frederick J.
  • Dumpit, Ronald F.
  • Deckwerth, Thomas L.
  • Wintner, Edward A.
  • Bathe, Duncan P.

Abstract

A controlled reactor for use in making pharmaceutical nitric oxide for inhalation by a patient. The reactor including a cassette having a hydrophilic porous substrate coated and impregnated with a particulate reductant such as croconic acid. The reactor also including a piezoelectric print head for atomizing and pulsing small droplets of an aqueous solution containing nitrite ions, non-detergent surfactant, and, viscosity agent. The reactor used to provide controlled delivery of pharmaceutical nitric oxide gas to a controlled patient inhalation delivery system that may include a mechanical ventilator circuit.

IPC Classes  ?

  • A61M 16/14 - Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
  • A61K 33/02 - AmmoniaCompounds thereof
  • A61M 16/12 - Preparation of respiratory gases or vapours by mixing different gases
  • A61K 9/72 - Medicinal preparations characterised by special physical form for smoking or inhaling

6.

METHODS FOR TREATING OR PREVENTING RADIOCONTRAST AGENT INDUCED KIDNEY INJURY

      
Application Number US2010021562
Publication Number 2010/090850
Status In Force
Filing Date 2010-01-21
Publication Date 2010-08-12
Owner IKARIA, INC, (USA)
Inventor
  • Su, Chienmin
  • Szabo, Csaba

Abstract

Methods for treating or preventing radiocontrast agent induced kidney injury in a mammal are disclosed, the methods comprising administering to the mammal a first effective amount of a chalcogenide composition prior to administering a radiocontrast agent to the mammal.

IPC Classes  ?

  • A61K 33/04 - Sulfur, selenium or telluriumCompounds thereof
  • A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
  • A61K 47/02 - Inorganic compounds
  • A61K 9/00 - Medicinal preparations characterised by special physical form

7.

COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING HYPOXIC OR ISCHEMIC INJURY

      
Application Number US2009061046
Publication Number 2010/045582
Status In Force
Filing Date 2009-10-16
Publication Date 2010-04-22
Owner IKARIA, INC. (USA)
Inventor
  • Wintner, Edward, Aurel
  • Ruan, Fuqiang

Abstract

A method for treating or preventing injury of a biological material exposed to hypoxic or ischemic conditions comprising contacting the biological material with an effective amount of a compound is disclosed. The compound has the following structure (I): R1_(S)n-R2 or a stereoisomer, pharmaceutically acceptable salt or prodrug thereof, wherein R1, R2, and n are as defined herein. Compounds, methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed.

IPC Classes  ?

  • C07C 321/00 - Thiols, sulfides, hydropolysulfides or polysulfides
  • A61K 31/10 - SulfidesSulfoxidesSulfones
  • A61K 31/105 - Persulfides
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 39/00 - General protective or antinoxious agents
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics

8.

COMPOSITIONS COMPRISING SULFIDE ALONE OR IN COMBINATION WITH NITRIC OXIDE AND THEIR USE TO

      
Application Number US2008066973
Publication Number 2008/157393
Status In Force
Filing Date 2008-06-13
Publication Date 2008-12-24
Owner IKARIA, INC. (USA)
Inventor Szabo, Csaba

Abstract

The present invention provides methods of stimulating angiogenesis and the growth or migration of cells associated with angiogenesis, by contacting animals, tissues, or cells with sulfide, alone or in combination with nitric oxide. These methods may be used for a variety of purposes, including promoting wound healing, increasing blood flow, and for the treatment and prevention of diseases and disorders associated with decreased blood flow, including ischemic or hypoxic injury.

IPC Classes  ?

  • A61K 33/00 - Medicinal preparations containing inorganic active ingredients
  • A61K 33/04 - Sulfur, selenium or telluriumCompounds thereof
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 39/00 - General protective or antinoxious agents

9.

COMBINATIONS OF NITRIC OXIDE AND SULFIDE AND METHODS OF USE AND MANUFACTURE THEREOF

      
Application Number US2007088402
Publication Number 2008/079993
Status In Force
Filing Date 2007-12-20
Publication Date 2008-07-03
Owner IKARIA, INC. (USA)
Inventor
  • Szabo, Csaba
  • Tomaselli, Kevin, J.

Abstract

The present invention provides methods of reducing the cytotoxic effects of nitric oxide and sulfides comprising coadministering nitric oxide with sulfide. In addition, the present invention provides novel pharmaceutical compositions comprising both nitric oxide and sulfide. The methods and compositions of the present invention may be used in the treatment or prevention of a variety of diseases and disorders, and also in the prevention of cell or tissue damage, including that resulting from ischemia or hypoxia.

IPC Classes  ?

  • A61K 33/00 - Medicinal preparations containing inorganic active ingredients
  • A61K 33/04 - Sulfur, selenium or telluriumCompounds thereof
  • A61M 16/12 - Preparation of respiratory gases or vapours by mixing different gases
  • A61P 39/00 - General protective or antinoxious agents

10.

COMPOSITIONS AND METHODS FOR ENHANCING SURVIVAL AND REDUCING INJURY UNDER ISCHEMIC OR HYPOXIC CONDITIONS

      
Application Number US2007086544
Publication Number 2008/070741
Status In Force
Filing Date 2007-12-05
Publication Date 2008-06-12
Owner IKARIA, INC. (USA)
Inventor
  • Wintner, Edward, Aurel
  • Szabo, Csaba
  • Tomaselli, Kevin, James
  • Deckwerth, Thomas, L.
  • Insko, Michael, A.
  • Johnson, Jeffrey, C.

Abstract

The present invention is directed to compositions and methods for enhancing the survivability of, and/or reducing damage to, cells, tissues, organs, and organisms, particularly under ischemic or hypoxic conditions.

IPC Classes  ?

  • A61K 31/54 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one sulfur as the ring hetero atoms, e.g. sulthiame
  • A61K 31/425 - Thiazoles
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 39/00 - General protective or antinoxious agents

11.

LIQUID CHALCOGENIDE COMPOSITIONS AND METHODS OF MANUFACTURING AND USING THE SAME

      
Application Number US2007080613
Publication Number 2008/043081
Status In Force
Filing Date 2007-10-05
Publication Date 2008-04-10
Owner IKARIA, INC. (USA)
Inventor
  • Tomaselli, Kevin, J.
  • Hill, Paul, A.
  • Deckwerth, Thomas, L.
  • Wintner, Edward
  • Szabo, Csaba

Abstract

The present invention provides novel stable, liquid compositions comprising chalcogenides or salts thereof. These compositions may be used for a variety of purposes, including the treatment and prevention of ischemic or hypoxic injury, as well as in the preservation of biological matter.

IPC Classes  ?

  • A61K 33/08 - OxidesHydroxides
  • A61K 47/12 - Carboxylic acidsSalts or anhydrides thereof
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 39/00 - General protective or antinoxious agents

12.

IKARIA

      
Application Number 004664652
Status Registered
Filing Date 2005-10-21
Registration Date 2006-09-06
Owner Ikaria, Inc. (USA)
NICE Classes  ?
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 10 - Medical apparatus and instruments
  • 42 - Scientific, technological and industrial services, research and design

Goods & Services

Pharmaceutical and veterinary preparations; sanitary preparations for medical purposes; dietetic substances adapted for medical use, food for babies; plasters, materials for dressings; material for stopping teeth, dental wax; disinfectants; preparations for destroying vermin; fungicides, herbicides; pharmaceutical preparations for medical treatment of critically ill patients who are suffering from cancer, heart attack, stroke, shock, trauma, and major surgery. Surgical, medical, dental and veterinary apparatus and instruments, artificial limbs, eyes and teeth; orthopedic articles; suture materials; medical devices for the treatment of organ transplantation. Scientific and technological services and research and design relating thereto; industrial analysis and research services; design and development of computer hardware and software; legal services; pharmaceutical research and development services for pharmaceutical preparations and medical devices.