HRP20121078T1 - Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura - Google Patents
Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura Download PDFInfo
- Publication number
- HRP20121078T1 HRP20121078T1 HRP20121078AT HRP20121078T HRP20121078T1 HR P20121078 T1 HRP20121078 T1 HR P20121078T1 HR P20121078A T HRP20121078A T HR P20121078AT HR P20121078 T HRP20121078 T HR P20121078T HR P20121078 T1 HRP20121078 T1 HR P20121078T1
- Authority
- HR
- Croatia
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- quinuclidin
- aminothiazol
- acetanilide
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title claims 9
- 206010020853 Hypertonic bladder Diseases 0.000 title claims 6
- 208000009722 Overactive Urinary Bladder Diseases 0.000 title claims 6
- 208000020629 overactive bladder Diseases 0.000 title claims 6
- 150000003839 salts Chemical class 0.000 claims 16
- PBAPPPCECJKMCM-IBGZPJMESA-N mirabegron Chemical compound S1C(N)=NC(CC(=O)NC=2C=CC(CCNC[C@H](O)C=3C=CC=CC=3)=CC=2)=C1 PBAPPPCECJKMCM-IBGZPJMESA-N 0.000 claims 9
- FBOUYBDGKBSUES-VXKWHMMOSA-N solifenacin Chemical compound C1([C@H]2C3=CC=CC=C3CCN2C(O[C@@H]2C3CCN(CC3)C2)=O)=CC=CC=C1 FBOUYBDGKBSUES-VXKWHMMOSA-N 0.000 claims 8
- 206010027566 Micturition urgency Diseases 0.000 claims 5
- 206010046543 Urinary incontinence Diseases 0.000 claims 5
- RXZMMZZRUPYENV-VROPFNGYSA-N Solifenacin succinate Chemical group OC(=O)CCC(O)=O.C1([C@H]2C3=CC=CC=C3CCN2C(O[C@@H]2C3CCN(CC3)C2)=O)=CC=CC=C1 RXZMMZZRUPYENV-VROPFNGYSA-N 0.000 claims 3
- -1 2-hydroxy-2-phenylethyl Chemical group 0.000 claims 2
- 206010036018 Pollakiuria Diseases 0.000 claims 2
- 229960001413 acetanilide Drugs 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000004615 ingredient Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- FZERHIULMFGESH-UHFFFAOYSA-N methylenecarboxanilide Natural products CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 238000000034 method Methods 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
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
- A61K31/33—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
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine 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
- A61K31/41—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
- A61K31/426—1,3-Thiazoles
-
- 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
-
- 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
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Claims (13)
1. Farmaceutski sastav, naznačen time, da kao djelotvorne sastojke uključuje (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid ili njegovu farmaceutski prihvatljivu sol i (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat ili njegovu farmaceutski prihvatljivu sol.
2. Farmaceutski sastav prema zahtjevu 1, naznačen time, da (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid ili njegova farmaceutski prihvatljiva sol je (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid.
3. Farmaceutski sastav prema zahtjevu 1 ili 2, naznačen time, da (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat ili njegova farmaceutski prihvatljiva sol je (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat sukcinat.
4. Farmaceutski sastav prema bilo kojem od zahtjeva 1 do 3, naznačen time, da nadalje uključuje farmaceutski prihvatljivo pomoćno sredstvo.
5. Farmaceutski sastav prema zahtjevu 1, naznačen time, da kao djelotvorne sastojke uključuje (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid ili njegovu farmaceutski prihvatljivu sol u količini od 10 do 100 mg u obliku (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilida, te (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat ili njegovu farmaceutski prihvatljivu sol u količini od 0,5 mg do 10 mg u obliku (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat sukcinata.
6. Farmaceutski sastav prema zahtjevu 5, naznačen time, da uključuje 10 mg do 100 mg od (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilida, i 0,5 mg do 10 mg od (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat sukcinata.
7. Farmaceutski sastav prema bilo kojem od zahtjeva 1 do 6, naznačen time, da je to pripravak za oralno davanje.
8. Farmaceutski sastav prema bilo kojem od zahtjeva 1 do 7, naznačen time, da se upotrebljava u postupku za liječenje urinarne urgencije, polakisurije i/ili urinarne inkontinencije koje su povezane s hiperaktivnim mjehurom.
9. Uporaba (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilata ili njegove farmaceutski prihvatljive soli, naznačena time, da je za proizvodnju terapeutskog sredstva koji se upotrebljava u kombinaciji s (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilidom ili njegovom farmaceutski prihvatljivom soli, a koji služi za liječenje urinarne urgencije, polakisurije i/ili urinarne inkontinencije koje su povezane s hiperaktivnim mjehurom.
10. Uporaba (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilida ili njegove farmaceutski prihvatljive soli, naznačena time, da je za proizvodnju terapeutskog sredstva koji se upotrebljava u kombinaciji s (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilatom ili njegovom farmaceutski prihvatljivom soli, a koji služi za liječenje urinarne urgencije, polakisurije i/ili urinarne inkontinencije koje su povezane s hiperaktivnim mjehurom.
11. (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid ili njegova farmaceutski prihvatljiva sol, naznačen time, da se upotrebljava u kombinaciji s (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilatom ili njegovom farmaceutski prihvatljivom soli, a služi za uporabu u postupku liječenja urinarne urgencije, polakisurije i/ili urinarne inkontinencije koje su povezane s hiperaktivnim mjehurom.
12. (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat ili njegova farmaceutski prihvatljiva sol, naznačen time, da se upotrebljava u kombinaciji s (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilidom ili njegovom farmaceutski prihvatljivom soli, a služi za uporabu u postupku liječenja urinarne urgencije, polakisurije i/ili urinarne inkontinencije koje su povezane s hiperaktivnim mjehurom.
13. Kombinacija za upotrebu prema zahtjevu 11 ili 12, naznačena time, da se (R)-2-(2-aminotiazol-4-il)-4’-{2-[(2-hidroksi-2-feniletil)amino]etil}acetanilid ili njegova farmaceutski prihvatljiva sol i (3R)-kinuklidin-3-il(1S)-1-fenil-1,2,3,4-tetrahidroizokinolin-2-karboksilat ili njegova farmaceutski prihvatljiva sol, primjenuju istovremeno, odvojeno ili uzastopno, ili u odabranim vremenskim intervalima.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007285802 | 2007-11-02 | ||
PCT/JP2008/069736 WO2009057685A1 (ja) | 2007-11-02 | 2008-10-30 | 過活動膀胱治療用医薬組成物 |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20121078T1 true HRP20121078T1 (hr) | 2013-01-31 |
Family
ID=40591069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HRP20121078AT HRP20121078T1 (hr) | 2007-11-02 | 2012-12-28 | Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura |
Country Status (12)
Country | Link |
---|---|
US (2) | US20100240697A1 (hr) |
EP (1) | EP2216021B1 (hr) |
JP (1) | JP5263170B2 (hr) |
CA (1) | CA2704298C (hr) |
CY (1) | CY1113670T1 (hr) |
DK (1) | DK2216021T3 (hr) |
ES (1) | ES2393525T3 (hr) |
HR (1) | HRP20121078T1 (hr) |
PL (1) | PL2216021T3 (hr) |
PT (1) | PT2216021E (hr) |
SI (1) | SI2216021T1 (hr) |
WO (1) | WO2009057685A1 (hr) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2807135C (en) * | 2010-08-03 | 2019-05-14 | Altherx, Inc. | Combinations of beta - 3 adrenergic receptor agonists and muscarinic receptor antagonists for treating overactive bladder |
US9522129B2 (en) | 2010-08-03 | 2016-12-20 | Velicept Therapeutics, Inc. | Pharmaceutical Combination |
US9907767B2 (en) | 2010-08-03 | 2018-03-06 | Velicept Therapeutics, Inc. | Pharmaceutical compositions and the treatment of overactive bladder |
US20150306090A1 (en) * | 2012-08-31 | 2015-10-29 | Astellas Pharma Inc. | Orally administered medical composition |
ES2750751T3 (es) * | 2014-09-09 | 2020-03-27 | Astellas Pharma Inc | Composición farmacéutica novedosa para la prevención y/o el tratamiento de la incontinencia urinaria |
KR20170086659A (ko) | 2014-12-03 | 2017-07-26 | 벨리셉트 테라퓨틱스, 인크. | 하부 요로 증상을 위한 변형 방출형 솔라베그론을 이용한 조성물 및 방법 |
US10065922B2 (en) | 2015-10-23 | 2018-09-04 | Velicept Therapeutics, Inc. | Solabegron zwitterion and uses thereof |
WO2017186598A1 (en) | 2016-04-25 | 2017-11-02 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
EP3448367A1 (en) | 2016-04-25 | 2019-03-06 | Synthon BV | Tablets comprising mirabegron and solifenacin |
US10478399B2 (en) | 2017-10-12 | 2019-11-19 | Synthon B.V. | Modified release tablet composition comprising mirabegron |
WO2022006336A1 (en) * | 2020-07-01 | 2022-01-06 | Jubilant Pharma Holdings Inc. | Long-acting injection dosage form of beta 3 adrenoreceptor agonists |
EP4159199A1 (en) | 2021-09-29 | 2023-04-05 | Lotus Pharmaceutical Co., Ltd. | Combined formulation of mirabegron and solifenacin |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NO2005012I1 (no) * | 1994-12-28 | 2005-06-06 | Debio Rech Pharma Sa | Triptorelin og farmasoytisk akseptable salter derav |
DE69823858T2 (de) | 1997-10-17 | 2005-04-28 | Yamanouchi Pharmaceutical Co., Ltd. | Amidderivate oder deren salze |
US7342117B2 (en) * | 2001-10-30 | 2008-03-11 | Astellas Pharma Inc. | α-form or β-form crystal of acetanilide derivative |
JP4466370B2 (ja) * | 2002-06-07 | 2010-05-26 | アステラス製薬株式会社 | 過活動膀胱治療剤 |
DE60336334D1 (de) | 2002-11-07 | 2011-04-21 | Astellas Pharma Inc | Mittel zur behandlung von blasenhyperaktivität mit einem essigsäureanilid-derivat als wirkstoff |
EP1424079A1 (en) | 2002-11-27 | 2004-06-02 | Boehringer Ingelheim International GmbH | Combination of a beta-3-receptor agonist and of a reuptake inhibitor of serotonin and/or norepinephrine |
ES2290741T3 (es) * | 2003-04-04 | 2008-02-16 | Dynogen Pharmaceuticals Inc. | Metodo de tratamiento de trastornos del tracto urinario inferior. |
EP1682183A2 (de) * | 2003-11-03 | 2006-07-26 | Boehringer Ingelheim International Gmbh | Pharmazeutische zusammensetzung enthaltend einen beta-3-adrenozeptor-agonisten und einem alpha antagonisten und/oder einen 5-alpha reduktase-hemmer |
EP1726304A4 (en) | 2004-03-16 | 2010-04-28 | Astellas Pharma Inc | COMPOSITION CONTAINING SOLIFENACIN |
US20090131469A1 (en) * | 2005-02-25 | 2009-05-21 | Astellas Pharma Inc. | Pharmaceutical agent comprising solifenacin |
EP1967202A1 (en) * | 2007-03-05 | 2008-09-10 | AEterna Zentaris GmbH | Use of LHRH Antagonists for the Treatment of Lower Urinary Tract Symptoms, in particular Overactive Bladder and/or Detrusor Overactivity |
-
2008
- 2008-10-30 PL PL08843784T patent/PL2216021T3/pl unknown
- 2008-10-30 PT PT08843784T patent/PT2216021E/pt unknown
- 2008-10-30 US US12/740,699 patent/US20100240697A1/en not_active Abandoned
- 2008-10-30 CA CA2704298A patent/CA2704298C/en active Active
- 2008-10-30 SI SI200830841T patent/SI2216021T1/sl unknown
- 2008-10-30 DK DK08843784.3T patent/DK2216021T3/da active
- 2008-10-30 ES ES08843784T patent/ES2393525T3/es active Active
- 2008-10-30 EP EP08843784A patent/EP2216021B1/en not_active Revoked
- 2008-10-30 JP JP2009539100A patent/JP5263170B2/ja active Active
- 2008-10-30 WO PCT/JP2008/069736 patent/WO2009057685A1/ja active Application Filing
-
2012
- 2012-12-28 HR HRP20121078AT patent/HRP20121078T1/hr unknown
-
2013
- 2013-01-04 CY CY20131100004T patent/CY1113670T1/el unknown
- 2013-01-24 US US13/748,956 patent/US8772315B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
EP2216021A4 (en) | 2010-11-03 |
CA2704298C (en) | 2015-07-21 |
PL2216021T3 (pl) | 2013-03-29 |
JP5263170B2 (ja) | 2013-08-14 |
ES2393525T3 (es) | 2012-12-26 |
US8772315B2 (en) | 2014-07-08 |
CY1113670T1 (el) | 2016-06-22 |
JPWO2009057685A1 (ja) | 2011-03-10 |
DK2216021T3 (da) | 2012-11-05 |
CA2704298A1 (en) | 2009-05-07 |
SI2216021T1 (sl) | 2013-01-31 |
PT2216021E (pt) | 2012-11-06 |
EP2216021B1 (en) | 2012-10-17 |
WO2009057685A1 (ja) | 2009-05-07 |
EP2216021A1 (en) | 2010-08-11 |
US20100240697A1 (en) | 2010-09-23 |
US20130150402A1 (en) | 2013-06-13 |
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