FR20C1022I2 - DOSAGE OF AN S1P RECEPTOR AGONIST - Google Patents
DOSAGE OF AN S1P RECEPTOR AGONISTInfo
- Publication number
- FR20C1022I2 FR20C1022I2 FR20C1022C FR20C1022C FR20C1022I2 FR 20C1022 I2 FR20C1022 I2 FR 20C1022I2 FR 20C1022 C FR20C1022 C FR 20C1022C FR 20C1022 C FR20C1022 C FR 20C1022C FR 20C1022 I2 FR20C1022 I2 FR 20C1022I2
- Authority
- FR
- France
- Prior art keywords
- dosage
- receptor agonist
- agonist
- receptor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—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
- A61K31/401—Proline; Derivatives thereof, e.g. captopril
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4458—Non condensed piperidines, e.g. piperocaine only substituted in position 2, e.g. methylphenidate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—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
- C07D211/36—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13967308P | 2008-12-22 | 2008-12-22 | |
| EP09167209 | 2009-08-04 | ||
| EP09793546.4A EP2379069B1 (en) | 2008-12-22 | 2009-12-21 | Dosage regimen of an s1p receptor agonist |
| PCT/EP2009/067618 WO2010072703A1 (en) | 2008-12-22 | 2009-12-21 | Dosage regimen of an s1p receptor agonist |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR20C1022I1 FR20C1022I1 (en) | 2020-07-31 |
| FR20C1022I2 true FR20C1022I2 (en) | 2021-06-11 |
Family
ID=41435196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR20C1022C Active FR20C1022I2 (en) | 2008-12-22 | 2020-06-18 | DOSAGE OF AN S1P RECEPTOR AGONIST |
Country Status (34)
| Country | Link |
|---|---|
| US (2) | US8492441B2 (en) |
| EP (1) | EP2379069B1 (en) |
| JP (2) | JP5657565B2 (en) |
| KR (1) | KR101660555B1 (en) |
| CN (2) | CN105213372A (en) |
| AR (1) | AR074825A1 (en) |
| AU (1) | AU2009331582B2 (en) |
| BR (1) | BRPI0923213A2 (en) |
| CA (3) | CA2981830A1 (en) |
| CY (2) | CY1116321T1 (en) |
| DK (1) | DK2379069T3 (en) |
| ES (1) | ES2538413T3 (en) |
| FR (1) | FR20C1022I2 (en) |
| HR (1) | HRP20150567T1 (en) |
| HU (2) | HUE026400T2 (en) |
| IL (2) | IL294658A (en) |
| JO (1) | JO3044B1 (en) |
| LT (1) | LTC2379069I2 (en) |
| LU (1) | LUC00160I2 (en) |
| MA (1) | MA32907B1 (en) |
| MX (2) | MX2011006625A (en) |
| NL (1) | NL301046I2 (en) |
| NO (1) | NO2020017I1 (en) |
| NZ (1) | NZ593427A (en) |
| PL (1) | PL2379069T3 (en) |
| PT (1) | PT2379069E (en) |
| RU (1) | RU2561681C2 (en) |
| SG (1) | SG171888A1 (en) |
| SI (1) | SI2379069T1 (en) |
| TN (1) | TN2011000281A1 (en) |
| TW (1) | TWI472327B (en) |
| UY (1) | UY32350A (en) |
| WO (1) | WO2010072703A1 (en) |
| ZA (1) | ZA201104102B (en) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101718639B1 (en) | 2008-03-17 | 2017-03-21 | 액테리온 파마슈티칼 리미티드 | Dosing Regimen for a Selective S1P1 Receptor Agonist |
| US9149459B2 (en) * | 2008-07-23 | 2015-10-06 | Novartis Ag | Sphingosine 1 phosphate receptor modulators and their use to treat muscle inflammation |
| HRP20151190T1 (en) | 2008-12-22 | 2016-01-01 | Novartis Ag | DOSAGE MODE FOR FINGOLIMOD IN TREATMENT OF MULTIPLE SCLEROSIS |
| SG10201500639TA (en) | 2010-01-27 | 2015-03-30 | Arena Pharm Inc | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| EP2566473B1 (en) * | 2010-05-06 | 2016-01-06 | Novartis AG | Dosage regimen of diaryl sulfide derivatives |
| EP2455080A1 (en) * | 2010-11-23 | 2012-05-23 | Almirall, S.A. | S1P1 receptor agonists for use in the treatment of multiple sclerosis |
| BR112013017302B1 (en) | 2011-01-07 | 2021-12-07 | Novartis Ag | PHARMACEUTICAL COMPOSITION IN SOLID PHASE |
| WO2012095853A1 (en) | 2011-01-10 | 2012-07-19 | Novartis Pharma Ag | Modified release formulations comprising sip receptor modulators |
| MX2014004813A (en) * | 2011-10-21 | 2014-05-20 | Novartis Ag | Dosage regimen for an s1p receptor modulator or agonist. |
| SI2885266T1 (en) | 2012-08-17 | 2020-10-30 | Actelion Pharmaceuticals Ltd | Process for the preparation of (2z,5z)-5-(3-chloro-4-((r)-2,3-dihydroxypropoxy)benzylidene)-2-(propylimino)-3-(o-tolyl)thiazolidin-4-one and intermediate used in said process |
| EP3199947A3 (en) * | 2013-04-04 | 2017-09-13 | Novartis AG | Identifying patient response to s1p receptor modulator administration |
| KR102466348B1 (en) * | 2014-04-10 | 2022-11-10 | 노파르티스 아게 | Immunosuppressant formulation |
| US20170027907A1 (en) | 2014-04-10 | 2017-02-02 | Eric Legangneux | Sip modulator immediate release dosage regimen |
| MA41139A (en) | 2014-12-11 | 2017-10-17 | Actelion Pharmaceuticals Ltd | PHARMACEUTICAL COMBINATION INCLUDING A SIP1 RECEPTOR SELECTIVE AGONIST |
| WO2016091996A1 (en) | 2014-12-11 | 2016-06-16 | Actelion Pharmaceuticals Ltd | Dosing regimen for a selective s1p1 receptor agonist |
| ES2995737T3 (en) * | 2015-01-06 | 2025-02-11 | Arena Pharm Inc | Compound for use in treating conditions related to the s1p1 receptor |
| US20180042895A1 (en) * | 2015-02-26 | 2018-02-15 | Novartis Ag | Treatment of autoimmune disease in a patient receiving additionally a beta-blocker |
| MA42807A (en) | 2015-06-22 | 2018-07-25 | Arena Pharm Inc | SALT L-ARGININE CRYSTALLINE ACID (R) -2- (7- (4-CYCLOPENTYL-3- (TRIFLUOROMETHYL) BENZYLOXY) -1,2,3,4-TETRAHYDROCYCLO-PENTA [B] INDOL-3-YL) ACETIC (COMPOUND 1) FOR USE IN CONDITIONS ASSOCIATED WITH THE S1P1 RECEIVER |
| CA3053416A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of inflammatory bowel disease with extra-intestinal manifestations |
| WO2018151873A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| US11629124B2 (en) | 2017-03-09 | 2023-04-18 | Novartis Ag | Solid forms comprising an oxime ether compound, compositions and methods of use thereof |
| US11434200B2 (en) | 2017-03-09 | 2022-09-06 | Novartis Ag | Solid forms comprising an oxime ether compound and a coformer, compositions and methods of use thereof |
| US11059784B2 (en) | 2017-08-09 | 2021-07-13 | Bristol-Myers Squibb Company | Oxime ether compounds |
| WO2019032632A1 (en) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | Alkylphenyl compounds |
| CN111107845A (en) * | 2017-09-29 | 2020-05-05 | 诺华股份有限公司 | Dosing regimen for cilnidimod |
| AU2018343239A1 (en) * | 2017-09-29 | 2020-03-12 | Novartis Ag | Dosing regimen of siponimod |
| EP3801459B1 (en) | 2018-06-06 | 2024-08-07 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the s1p1 receptor |
| PH12022551043A1 (en) | 2019-10-31 | 2023-05-03 | Idorsia Pharmaceuticals Ltd | Combination of a cxcr7 antagonist with an s1p1 receptor modulator |
| US11135197B2 (en) | 2020-02-07 | 2021-10-05 | Argentum Pharmaceuticals Llc | Dosage regimen of an S1P receptor modulator |
| WO2021158848A1 (en) * | 2020-02-07 | 2021-08-12 | Argentum Pharmaceuticals Llc | Dosage regimen of an s1p receptor agonist |
| JP2024506041A (en) | 2021-02-08 | 2024-02-08 | ボシュ ヘルス アイルランド リミテッド | Amicelimod to prevent, treat, or ameliorate ulcerative colitis |
| EP4212156A1 (en) | 2022-01-13 | 2023-07-19 | Abivax | Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a s1p receptor modulator |
| WO2025134072A1 (en) | 2023-12-21 | 2025-06-26 | Bausch Health Ireland Limited | Methods for preventing, treating, or ameliorating ulcerative colitis in certain patient populations with amiselimod |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1176819A (en) * | 1997-09-03 | 1998-03-25 | 王树生 | Sobering beverage and method for preparing same |
| ES2316758T3 (en) | 2002-05-16 | 2009-04-16 | Novartis Ag | USE OF EDG RECEIVER BINDERS IN CANCER. |
| PE20050158A1 (en) | 2003-05-19 | 2005-05-12 | Irm Llc | IMMUNOSUPPRESSOR COMPOUNDS AND COMPOSITIONS |
| MY150088A (en) * | 2003-05-19 | 2013-11-29 | Irm Llc | Immunosuppressant compounds and compositions |
| US20050095292A1 (en) * | 2003-10-29 | 2005-05-05 | Wyeth | Sustained release pharmaceutical compositions |
| US20070099891A1 (en) | 2003-12-17 | 2007-05-03 | Kouichi Kino | Medicinal compositions and combinations |
| UA74941C2 (en) | 2004-04-26 | 2006-02-15 | Fos Internat S A | A metal-thermal process for producing magnesium and vacuum induction furnace for realizing the same |
| WO2005113330A1 (en) | 2004-05-05 | 2005-12-01 | Adler, Richard, S. | Systems and methods for protecting ship from attack on the surface or under water |
| KR20130041385A (en) * | 2004-11-29 | 2013-04-24 | 노파르티스 아게 | Dosage regimen of an s1p receptor agonist |
| RU2008113439A (en) * | 2005-09-09 | 2009-10-20 | Лабофарм Инк. (CA) | COMPOSITIONS WITH SLOW DELIVERY OF A MEDICINAL PRODUCT |
| WO2008072056A1 (en) * | 2006-12-14 | 2008-06-19 | Pfizer Limited | Use of mtp inhibitors for the treatment of obesity using low doses and dose-escalation |
| DE102007019417A1 (en) * | 2007-04-23 | 2008-11-13 | Grünenthal GmbH | Tapentadol for the treatment of pain in osteoarthritis |
| AR068986A1 (en) * | 2007-10-12 | 2009-12-23 | Novartis Ag | COMPOSITIONS THAT INCLUDE MODULATORS OF THE SPHINGOSINE-1 PHOSPHATE RECEIVER (S1P) |
-
2009
- 2009-12-21 JP JP2011541496A patent/JP5657565B2/en active Active
- 2009-12-21 MX MX2011006625A patent/MX2011006625A/en active IP Right Grant
- 2009-12-21 AR ARP090105009A patent/AR074825A1/en unknown
- 2009-12-21 WO PCT/EP2009/067618 patent/WO2010072703A1/en not_active Ceased
- 2009-12-21 JO JOP/2009/0495A patent/JO3044B1/en active
- 2009-12-21 CA CA2981830A patent/CA2981830A1/en not_active Abandoned
- 2009-12-21 EP EP09793546.4A patent/EP2379069B1/en active Active
- 2009-12-21 ES ES09793546.4T patent/ES2538413T3/en active Active
- 2009-12-21 SG SG2011039765A patent/SG171888A1/en unknown
- 2009-12-21 AU AU2009331582A patent/AU2009331582B2/en active Active
- 2009-12-21 MX MX2015011590A patent/MX367667B/en unknown
- 2009-12-21 TW TW98143961A patent/TWI472327B/en active
- 2009-12-21 CA CA2747992A patent/CA2747992C/en active Active
- 2009-12-21 PL PL09793546T patent/PL2379069T3/en unknown
- 2009-12-21 RU RU2011129856/15A patent/RU2561681C2/en active
- 2009-12-21 CN CN201510541635.7A patent/CN105213372A/en active Pending
- 2009-12-21 HR HRP20150567TT patent/HRP20150567T1/en unknown
- 2009-12-21 CN CN2009801519427A patent/CN102264363A/en active Pending
- 2009-12-21 DK DK09793546.4T patent/DK2379069T3/en active
- 2009-12-21 HU HUE09793546A patent/HUE026400T2/en unknown
- 2009-12-21 KR KR1020117017072A patent/KR101660555B1/en not_active Expired - Fee Related
- 2009-12-21 CA CA3105857A patent/CA3105857C/en active Active
- 2009-12-21 SI SI200931199T patent/SI2379069T1/en unknown
- 2009-12-21 IL IL294658A patent/IL294658A/en unknown
- 2009-12-21 NZ NZ593427A patent/NZ593427A/en not_active IP Right Cessation
- 2009-12-21 UY UY0001032350A patent/UY32350A/en not_active Application Discontinuation
- 2009-12-21 BR BRPI0923213A patent/BRPI0923213A2/en not_active IP Right Cessation
- 2009-12-21 PT PT97935464T patent/PT2379069E/en unknown
- 2009-12-22 US US12/655,049 patent/US8492441B2/en active Active
-
2011
- 2011-05-31 TN TN2011000281A patent/TN2011000281A1/en unknown
- 2011-06-02 ZA ZA2011/04102A patent/ZA201104102B/en unknown
- 2011-06-02 IL IL21334711A patent/IL213347B/en active IP Right Grant
- 2011-06-17 MA MA33953A patent/MA32907B1/en unknown
-
2013
- 2013-06-18 US US13/920,406 patent/US20130281712A1/en not_active Abandoned
-
2014
- 2014-09-19 JP JP2014191541A patent/JP5941110B2/en active Active
-
2015
- 2015-05-27 CY CY20151100469T patent/CY1116321T1/en unknown
-
2020
- 2020-06-16 NL NL301046C patent/NL301046I2/en unknown
- 2020-06-17 HU HUS2000017C patent/HUS2000017I1/en unknown
- 2020-06-17 NO NO2020017C patent/NO2020017I1/en unknown
- 2020-06-18 FR FR20C1022C patent/FR20C1022I2/en active Active
- 2020-06-18 LU LU00160C patent/LUC00160I2/fr unknown
- 2020-06-19 CY CY2020014C patent/CY2020014I2/en unknown
- 2020-06-23 LT LTPA2020513C patent/LTC2379069I2/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR20C1022I2 (en) | DOSAGE OF AN S1P RECEPTOR AGONIST | |
| FR25C1012I1 (en) | DOSAGE OF AN S1P RECEPTOR AGONIST | |
| MA29034B1 (en) | DOSAGE OF S1P RECEPTOR AGONIST | |
| FR22C1044I1 (en) | CGRP RECEPTOR ANTAGONISTS | |
| EP2150115A4 (en) | RECEPTOR ANTAGONISTS OF CYCLOPROPYLPYRROLIDINE OREXINE | |
| HUS1800027I1 (en) | Combinations of muscarinic receptor antagonist and beta-2-adrenoreceptor agonist | |
| KR101522157B9 (en) | Dosage of CMT inhibitors | |
| DK2252581T3 (en) | CAPE-SELECTIVE OPIOID RECEPTOR ANTAGONIST | |
| DK2421849T3 (en) | Diamide compounds with muscarinic receptor antagonist and beta2-adrenoreceptor agonist activity | |
| EP2427430A4 (en) | ANTAGONIST COMPOUNDS OF 5-OXO-SUMMER RECEPTORS | |
| EP2773352A4 (en) | 4-ARYLPIPERAZINE 1-SUBSTITUTED AS ANTAGONIST OF OPIOID RECEPTOR KAPPA | |
| PL2590992T3 (en) | Mu opioid receptor agonist analogs of the endomorphins | |
| EP2730290A4 (en) | TRANSDERMAL STAMP COMPRISING AN ANTAGONIST OF SEROTONIN RECEPTORS | |
| EP2249833A4 (en) | CGRP RECEPTOR ANTAGONIST PRODRUGS | |
| EP2271346A4 (en) | ANTAGONISTS OF MONOCYCLIC CGRP RECEPTORS | |
| EP2365748A4 (en) | IMIDAZOISOINDOLA ANTAGONISTS OF NEUROPEPTIDE S RECEPTORS | |
| EP2539706A4 (en) | ARYLPIPERAZONE ANTAGONISTS OF OPIOID RECEPTORS | |
| EP2341919A4 (en) | CGRP RECEPTOR ANTAGONISTS | |
| EP2089019A4 (en) | POLYMORPHS OF AN ANTAGONIST OF TACHYKININ HYDRO-ISO-INDOLIC RECEPTORS | |
| EP2331101A4 (en) | MONOCYCLIC AMIDE CGRP RECEPTOR ANTAGONISTS | |
| EP2339919A4 (en) | ANTAGONISTS OF CGRP RECEPTORS BASED ON BICYCLIC DIHYDROIMIDAZOLONE | |
| BRPI1014548A2 (en) | Methods of Administration of Thrombopoietin Agonist Compounds | |
| TH0901005765A (en) | Size specifications for S1P Receptor Agonist | |
| UA17747S (en) | DEVICE FOR INSPECTION OF PIPELINES "GNOM-100 D" |