WO2009063202A3 - Use of crth2 antagonist compounds - Google Patents
Use of crth2 antagonist compounds Download PDFInfo
- Publication number
- WO2009063202A3 WO2009063202A3 PCT/GB2008/003824 GB2008003824W WO2009063202A3 WO 2009063202 A3 WO2009063202 A3 WO 2009063202A3 GB 2008003824 W GB2008003824 W GB 2008003824W WO 2009063202 A3 WO2009063202 A3 WO 2009063202A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- antagonist compounds
- crth2 antagonist
- administered
- patient
- compound
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/14—Decongestants or antiallergics
-
- 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
- A61P37/08—Antiallergic agents
-
- 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
Abstract
The invention relates to compounds of general formula (I) wherein R1, R2, R3, R4 and R5 are as defined herein for the treatment of allergic conditions, wherein the treatment is by pulsed therapy which comprises a first period during which the compound is administered to the patient and a second period of at least seven days during which the compound is administered to the patient in a reduced amount.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010532660A JP2011503045A (en) | 2007-11-13 | 2008-11-13 | Use of CRTH2 antagonistic compounds |
DE08851028T DE08851028T1 (en) | 2007-11-13 | 2008-11-13 | USE OF CRTH2 ANTAGONIST COMPOUNDS |
EP08851028A EP2219645A2 (en) | 2007-11-13 | 2008-11-13 | Use of crth2 antagonist compounds |
US12/779,638 US20110124683A1 (en) | 2007-11-13 | 2010-05-13 | Use of CRTH2 Antagonist Compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0722203.7 | 2007-11-13 | ||
GBGB0722203.7A GB0722203D0 (en) | 2007-11-13 | 2007-11-13 | Use of CRTH2 antagonist compounds |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2008/003843 Continuation-In-Part WO2009063215A2 (en) | 2007-11-13 | 2008-11-13 | Use of crth2 antagonist compounds |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/779,638 Continuation-In-Part US20110124683A1 (en) | 2007-11-13 | 2010-05-13 | Use of CRTH2 Antagonist Compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009063202A2 WO2009063202A2 (en) | 2009-05-22 |
WO2009063202A3 true WO2009063202A3 (en) | 2009-08-27 |
Family
ID=38858584
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2008/003824 WO2009063202A2 (en) | 2007-11-13 | 2008-11-13 | Use of crth2 antagonist compounds |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP2219645A2 (en) |
JP (1) | JP2011503045A (en) |
DE (1) | DE08851028T1 (en) |
ES (1) | ES2353055T1 (en) |
GB (1) | GB0722203D0 (en) |
WO (1) | WO2009063202A2 (en) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT2327693E (en) * | 2007-12-14 | 2012-07-24 | Pulmagen Therapeutics Asthma Ltd | Indoles and their therapeutic use |
WO2009090414A1 (en) * | 2008-01-18 | 2009-07-23 | Oxagen Limited | Compounds having crth2 antagonist activity |
US7750027B2 (en) | 2008-01-18 | 2010-07-06 | Oxagen Limited | Compounds having CRTH2 antagonist activity |
JP2011509990A (en) * | 2008-01-22 | 2011-03-31 | オキサジェン リミテッド | Compound having CRTH2 antagonist activity |
EP2240444A1 (en) * | 2008-01-22 | 2010-10-20 | Oxagen Limited | Compounds having crth2 antagonist activity |
BRPI0907364A2 (en) | 2008-02-01 | 2015-07-14 | Amira Pharmaceuticals Inc | N, n-disubstituted aminoalkylbiphenyl prostaglandin d2 receptor antagonists |
JP2011512359A (en) | 2008-02-14 | 2011-04-21 | アミラ ファーマシューティカルズ,インク. | Cyclic diaryl ether compounds as antagonists of prostaglandin D2 receptors |
US8426449B2 (en) | 2008-04-02 | 2013-04-23 | Panmira Pharmaceuticals, Llc | Aminoalkylphenyl antagonists of prostaglandin D2 receptors |
WO2010008864A2 (en) | 2008-06-24 | 2010-01-21 | Amira Pharmaceuticals, Inc. | Cycloalkane[b]indole angtagonists of prostaglandin d2 receptors |
CN102076661B (en) | 2008-07-03 | 2014-04-09 | 潘米拉制药公司 | Antagonists of prostaglandin d2 receptors |
GB2463788B (en) | 2008-09-29 | 2010-12-15 | Amira Pharmaceuticals Inc | Heteroaryl antagonists of prostaglandin D2 receptors |
GB2465062B (en) | 2008-11-06 | 2011-04-13 | Amira Pharmaceuticals Inc | Cycloalkane(B)azaindole antagonists of prostaglandin D2 receptors |
US8383654B2 (en) | 2008-11-17 | 2013-02-26 | Panmira Pharmaceuticals, Llc | Heterocyclic antagonists of prostaglandin D2 receptors |
EP2461809A4 (en) | 2009-07-31 | 2013-06-19 | Panmira Pharmaceuticals Llc | Ophthalmic pharmaceutical compositions of dp2 receptor antagonists |
SG10201404662YA (en) | 2009-08-05 | 2014-10-30 | Panmira Pharmaceuticals Llc | Dp2 antagonist and uses thereof |
KR20120115989A (en) | 2010-01-06 | 2012-10-19 | 판미라 파마슈티칼스, 엘엘씨 | Dp2 antagonist and uses thereof |
KR101444572B1 (en) | 2010-03-22 | 2014-09-24 | 액테리온 파마슈티칼 리미티드 | 3-(heteroaryl-amino)-1,2,3,4-tetrahydro-9h-carbazole derivatives and their use as prostaglandin d2 receptor modulators |
JP5952829B2 (en) * | 2010-12-23 | 2016-07-13 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | Quinoxalines and aza-quinoxalines as CRTH2 receptor modulators |
GB201103837D0 (en) | 2011-03-07 | 2011-04-20 | Oxagen Ltd | Amorphous (5-Fluoro-2-Methyl-3-Quinolin-2-Ylmethyl-Indol-1-Yl)-acetic acid |
ES2596581T3 (en) | 2011-04-14 | 2017-01-10 | Actelion Pharmaceuticals Ltd. | Derivatives of 7- (heteroaryl-amino) -6,7,8,9-tetrahydropyridido [1,2-a] indole acetic acid and its use as modulators of the prostaglandin D2 receptor |
CN103086943B (en) * | 2011-11-04 | 2015-04-15 | 山东亨利医药科技有限责任公司 | Indoles derivative functioning as CRTH2 receptor antagonist |
MY179356A (en) | 2014-03-17 | 2020-11-05 | Idorsia Pharmaceuticals Ltd | Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators |
CA2938107A1 (en) | 2014-03-18 | 2015-09-24 | Actelion Pharmaceuticals Ltd | Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators |
GB201407820D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
GB201407807D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
TWI711616B (en) | 2015-09-15 | 2020-12-01 | 瑞士商愛杜西亞製藥有限公司 | Crystalline forms |
JPWO2017104728A1 (en) * | 2015-12-16 | 2018-11-29 | 幸久 村田 | Food allergy medicine |
EP3489233B1 (en) * | 2016-07-21 | 2022-01-12 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Indole derivative used as crth2 inhibitor |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005044260A1 (en) * | 2003-10-23 | 2005-05-19 | Oxagen Limited | Use of crth2 antagonist compounds in therapy |
WO2006092579A1 (en) * | 2005-03-01 | 2006-09-08 | Oxagen Limited | Microcrystalline ( 5-fluoro-2-methyl-3-quinolin-2-ylmethyl-indol-1-yl) acetic acid |
WO2006095183A1 (en) * | 2005-03-11 | 2006-09-14 | Oxagen Limited | 1-acetic acid-indole derivatives with pgd2 antagonist activity |
WO2007107772A1 (en) * | 2006-03-22 | 2007-09-27 | Oxagen Limited | Salts with crth2 antagonist activity |
WO2008012511A1 (en) * | 2006-07-22 | 2008-01-31 | Oxagen Limited | Compounds having crth2 antagonist activity |
-
2007
- 2007-11-13 GB GBGB0722203.7A patent/GB0722203D0/en not_active Ceased
-
2008
- 2008-11-13 WO PCT/GB2008/003824 patent/WO2009063202A2/en active Application Filing
- 2008-11-13 JP JP2010532660A patent/JP2011503045A/en active Pending
- 2008-11-13 EP EP08851028A patent/EP2219645A2/en not_active Ceased
- 2008-11-13 DE DE08851028T patent/DE08851028T1/en active Pending
- 2008-11-13 ES ES08851028T patent/ES2353055T1/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005044260A1 (en) * | 2003-10-23 | 2005-05-19 | Oxagen Limited | Use of crth2 antagonist compounds in therapy |
WO2006092579A1 (en) * | 2005-03-01 | 2006-09-08 | Oxagen Limited | Microcrystalline ( 5-fluoro-2-methyl-3-quinolin-2-ylmethyl-indol-1-yl) acetic acid |
WO2006095183A1 (en) * | 2005-03-11 | 2006-09-14 | Oxagen Limited | 1-acetic acid-indole derivatives with pgd2 antagonist activity |
WO2007107772A1 (en) * | 2006-03-22 | 2007-09-27 | Oxagen Limited | Salts with crth2 antagonist activity |
WO2008012511A1 (en) * | 2006-07-22 | 2008-01-31 | Oxagen Limited | Compounds having crth2 antagonist activity |
Non-Patent Citations (3)
Title |
---|
ANONYMOUS: "View of NCT00290381 on 2006_02_10", CLINICALTRIALS.GOV ARCHIVE, 10 February 2006 (2006-02-10), XP002534990, Retrieved from the Internet <URL:http://clinicaltrials.gov/archive/NCT00290381/2006_02_10> * |
ANONYMOUS: "View of NCT00697281 on 2008_06_12", CLINICAL TRIALS.GOV ARCHIVE, 12 June 2008 (2008-06-12), XP002535051, Retrieved from the Internet <URL:http://clinicaltrials.gov/archive/NCT00697281/2008_06_12> * |
See also references of EP2219645A2 * |
Also Published As
Publication number | Publication date |
---|---|
WO2009063202A2 (en) | 2009-05-22 |
DE08851028T1 (en) | 2011-02-24 |
GB0722203D0 (en) | 2007-12-19 |
JP2011503045A (en) | 2011-01-27 |
ES2353055T1 (en) | 2011-02-25 |
EP2219645A2 (en) | 2010-08-25 |
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