MSD Oss B.V.

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        Trademark 1
IPC Class
A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID] 3
A61K 31/4725 - Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings 2
A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems 2
A61P 25/18 - Antipsychotics, i.e. neurolepticsDrugs for mania or schizophrenia 2
A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia 2
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1.

BIOASSAYS FOR DETERMINING PD-1 MODULATION

      
Application Number US2011044798
Publication Number 2012/018538
Status In Force
Filing Date 2011-07-21
Publication Date 2012-02-09
Owner
  • MERCK SHARP & DOHME CORP. (USA)
  • MSD OSS B.V. (Netherlands)
Inventor
  • Carven, Gregory, John
  • Dulos, Gradus, Johannes
  • Elassaiss-Schaap, Jeroen

Abstract

The present invention relates to the identification and use of cytokine markers in bioassays for use in monitoring, diagnostic, patient selection, and treatment regimens involving blockade of the PD-1 pathway. In certain aspects, the invention provides methods and kits relating to these bioassays for selection and/or monitoring of treatment regimens involving PD-1 blockade. Biomarkers, kits, treatment regimens, therapeutic monitoring, and diagnostic methods related to anti-PD-1 therapies are provided.

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

2.

(11β,17α)-11-(4-(2-11C-ACETYL)PHENYL)-17,23-EPOXY- 19,24-DINORCHOLA-4,9,20-TRIEN-3-ONE

      
Application Number EP2011003012
Publication Number 2011/157443
Status In Force
Filing Date 2011-06-17
Publication Date 2011-12-22
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Brands, Franciscus Theodorus Leonardus
  • Hamersma, Johannes, Antonius, Maria
  • Wiegerinck, Peter, Hermanus, Gerardus

Abstract

The present invention relates to (11β,17α)-11-(4-(2-11C-acetyl)phenyl)-17,23- epoxy-19,24-dinorchola-4,9,20-trien-3-one, an 11C-labelled ORG 33628; a process for the preparation thereof, intermediates used in this process and the use of this compound as a PET tracer for the detection of breast cancer.

IPC Classes  ?

  • C07J 21/00 - Normal steroids containing carbon, hydrogen, halogen, or oxygen, having an oxygen-containing hetero ring spiro-condensed with the cyclopenta[a]hydrophenanthrene skeleton
  • A61K 31/58 - Compounds containing cyclopenta[a]hydrophenanthrene ring systemsDerivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
  • G01N 33/74 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving hormones
  • A61P 5/36 - Antigestagens

3.

THIENO (2, 3B) PYRAZINE COMPOUNDS AS B - RAF INHIBITORS

      
Application Number EP2011058329
Publication Number 2011/147764
Status In Force
Filing Date 2011-05-23
Publication Date 2011-12-01
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Folmer, Brigitte, Johanna, Bernita
  • Man, De, Adrianus, Petrus, Antonius
  • Gernette, Elisabeth, Sophia
  • Corte Real Gonçalves Azevedo, Rita
  • Ibrahim, Hemen

Abstract

The invention relates to compounds according to general Formula (I) or a pharmaceutically acceptable salt thereof. The compounds can be used for the treatment of cancer.

IPC Classes  ?

  • C07D 495/04 - Ortho-condensed systems
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
  • A61P 35/00 - Antineoplastic agents

4.

8-METHYL-1-PHENYL-IMIDAZOL[1,5-A]PYRAZINE COMPOUNDS

      
Application Number EP2011051584
Publication Number 2011/095556
Status In Force
Filing Date 2011-02-03
Publication Date 2011-08-11
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Man De,, Adrianus Petrus Antonius
  • Rewinkel,, Johannes Bernardus Maria
  • Jans,, Christiaan Gerardus Johannes Maria
  • Raaijmakers,, Hans Cornelis Andreas
  • Wijkmans,, Jacobus Cornelis Henricus Maria

Abstract

The present invention provides 8-methyl-1 -phenyl-imidazo[1,5-a]pyrazine derivatives according to formula I or pharmaceutically acceptable salts thereof. The compounds of the current invention show inhibitory activity against Lck and can be used for the treatment of Lck-mediated diseases or Lck-mediated conditions such as inflammatory disorders.

IPC Classes  ?

  • C07D 487/04 - Ortho-condensed systems
  • C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
  • A61K 31/4985 - Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 37/00 - Drugs for immunological or allergic disorders

5.

1H-[1,2,3]TRIAZOLO[4,5-c]PYRIDINE-4-CARBONITRILE DERIVATIVES

      
Application Number EP2011050393
Publication Number 2011/086125
Status In Force
Filing Date 2011-01-13
Publication Date 2011-07-21
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Cai, Jiaqiang
  • Bennett, David, Jonathan
  • Jones, Philip, Stephen

Abstract

The invention relates to 1H-[1,2,3]triazolo[4,5-c]pyridine-4-carbonitrile derived Cathepsin S inhibitors of Formula (I), wherein R1 is H or (C1-3)alkyl; R2 is halogen or (C1-4)alkyl, optionally substituted with one or more halogens; n is 1 -3; X is O or CH2; U, V and W are CH; or one of U, V and W is N; Y is a group capable of interacting with the Sn....S2 substites of the active site of Cathepsin S; or a pharmaceutically acceptable salt thereof, to pharmaceutical compositions comprising the same as well as to the use of these derivatives for the preparation of a medicament for the treatment of cathepsin S related diseases such as atherosclerosis, obesity, inflammation and immune disorders, such as rheumatoid arthritis, psoriasis, cancer, and chronic pain, such as neuropathic pain.

IPC Classes  ?

  • C07D 471/04 - Ortho-condensed systems
  • A61K 31/437 - 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]

6.

AMINO-HETEROARYL DERIVATIVES AS HCN BLOCKERS

      
Application Number EP2010070213
Publication Number 2011/076723
Status In Force
Filing Date 2010-12-20
Publication Date 2011-06-30
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Grove, Simon James Anthony
  • Morrison, Angus John
  • Jamieson, Craig
  • Palin, Ronald
  • Maclean, John Kinnaird Ferguson

Abstract

The invention relates to amino-heteroaryl derivatives having the general Formula I or a pharmaceutically acceptable salt thereof, to pharmaceutical compositions comprising the same, as well as to the use of these derivatives for the treatment of pain, such as neuropathic pain or inflammatory pain.

IPC Classes  ?

  • C07D 213/73 - Unsubstituted amino or imino radicals
  • C07D 239/42 - One nitrogen atom
  • C07D 401/12 - 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 chain containing hetero atoms as chain links
  • 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
  • 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
  • A61K 31/497 - Non-condensed pyrazines containing further heterocyclic rings
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61K 31/53 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
  • A61P 25/00 - Drugs for disorders of the nervous system

7.

MK2 INHIBITORS

      
Application Number EP2010069465
Publication Number 2011/073119
Status In Force
Filing Date 2010-12-13
Publication Date 2011-06-23
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Barf, Tjeerd Andries
  • Oubrie, Arthur
  • Schultz - Fademrecht, Carsten
  • Zwart, Eduard Willem
  • Hoogenboom, Niels
  • De Wilde, Sander Martijn
  • Kaptein, Allard

Abstract

The present invention relates to compounds of general Formula (I) or a pharmaceutically acceptable salt thereof. The compounds can be used in the treatment of immune, autoimmune, inflammatory diseases, cardiovascular diseases, infectious diseases, bone resorption disorders, neurodegenerative diseases or proliferative diseases.

IPC Classes  ?

  • C07D 471/20 - Spiro-condensed systems
  • A61K 31/438 - 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 the ring being spiro-condensed with carbocyclic or heterocyclic ring systems
  • A61P 37/02 - Immunomodulators
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • A61P 31/00 - Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P 19/08 - Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
  • A61P 35/00 - Antineoplastic agents

8.

HETEROCYLIC COMPOUNDS AS ANTAGONISTS OF THE OREXIN RECEPTORS

      
Application Number EP2010067904
Publication Number 2011/061318
Status In Force
Filing Date 2010-11-22
Publication Date 2011-05-26
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Bingham, Matilda Jane
  • Dunbar, Neil Andrew
  • Huggett, Margaret Jean
  • Wishart, Grant

Abstract

The present invention relates to a heterocyclic derivative according to formula (I) wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceutical composition comprising said heterocyclic derivatives and to their use in therapy, for instance in the treatment or prevention of disorders or diseases influenced by modulation of orexins, such as sleep disorders.

IPC Classes  ?

  • C07D 217/26 - Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
  • 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 471/04 - Ortho-condensed systems
  • A61K 31/4375 - 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring hetero atom, e.g. quinolizines, naphthyridines, berberine, vincamine
  • A61K 31/4725 - Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
  • A61K 31/55 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole

9.

(1,1, 1,3, 3, 3-HEXAFLUORO-2-HYDROXYPROPAN-2-YL) PHENYL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS THEREOF AND THEIR USE FOR THE TREATMENT OF ATHEROSCLEROSIS

      
Application Number EP2010066157
Publication Number 2011/051282
Status In Force
Filing Date 2010-10-26
Publication Date 2011-05-05
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Cooke, Andrew John
  • Carswell, Emma Louise
  • Bennett, David, Jonathan

Abstract

The present invention relates to (1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl derivatives having the general formula (I) to pharmaceutical compositions comprising the same and to the use of these (1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl derivatives in the treatment of atherosclerosis.

IPC Classes  ?

  • C07D 211/28 - Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms to which a second hetero atom is attached
  • C07D 213/75 - Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
  • C07D 237/20 - Nitrogen atoms
  • C07D 239/42 - One nitrogen atom
  • C07D 261/12 - Oxygen atoms
  • C07D 295/192 - Radicals derived from carboxylic acids from aromatic carboxylic acids
  • C07D 295/135 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
  • C07D 295/096 - Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
  • A61K 31/445 - Non-condensed piperidines, e.g. piperocaine
  • A61K 31/45 - Non-condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
  • A61K 31/4523 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems

10.

HETEROCYCLIC DERIVATIVES

      
Application Number EP2010066584
Publication Number 2011/051490
Status In Force
Filing Date 2010-11-02
Publication Date 2011-05-05
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Adam, Julia
  • Gillespie, Jonathan
  • Laats, Steven
  • Maclean, John Kinnaird Ferguson
  • Mcarthur, Duncan Robert

Abstract

The present invention relates to a heterocyclic derivative of formula (I) wherein the variables are as defined in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention further relates to pharmaceutical compositions comprising said heterocyclic derivatives and to their use in therapy, for instance in the treatment or prevention of disorders mediated by glutamate dysfunction, such as schizophrenia and generalised anxiety disorder.

IPC Classes  ?

  • C07D 401/10 - 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 aromatic rings
  • 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
  • C07D 405/14 - 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 three or more hetero rings
  • C07D 413/10 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
  • A61K 31/4178 - 1,3-Diazoles not condensed and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
  • A61K 31/422 - Oxazoles not condensed and containing further heterocyclic rings
  • 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
  • A61K 31/4725 - Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
  • A61P 25/18 - Antipsychotics, i.e. neurolepticsDrugs for mania or schizophrenia
  • A61P 25/22 - Anxiolytics

11.

CONDENSED AZINE - DERIVATIVES FOR THE TREATMENT OF DISEASES RELATED TO THE ACETYLCHOLINE RECEPTOR

      
Application Number EP2010065160
Publication Number 2011/045258
Status In Force
Filing Date 2010-10-11
Publication Date 2011-04-21
Owner MSD OSS B.V. (Netherlands)
Inventor
  • Ratcliffe, Paul David
  • Clarkson, Thomas Russell
  • Jeremiah, Fiona
  • Maclean, John Kinnaird Ferguson

Abstract

The present invention relates to a heterocyclic derivative of formula (I) wherein the variables are as defined in the specification or to a pharmaceutically acceptable salt or solvate thereof. The present invention further relates to pharmaceutical compositions comprising said heterocyclic derivatives and to their use in therapy, for instance in the treatment or prevention of disorders mediated by nicotinic acetylcholine receptors, such as schizophrenia and Alzheimer's disease.

IPC Classes  ?

  • C07D 471/08 - Bridged systems
  • A61K 31/551 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogens as ring hetero atoms, e.g. clozapine, dilazep
  • A61P 25/18 - Antipsychotics, i.e. neurolepticsDrugs for mania or schizophrenia
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

12.

NORCURON

      
Application Number 496962
Status Registered
Filing Date 1985-08-28
Registration Date 1985-08-28
Owner MSD Oss B.V. (Netherlands)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations and medicines for human use.