HRP20121078T1 - Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura - Google Patents

Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura Download PDF

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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
Application number
HRP20121078AT
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English (en)
Inventor
Masanori Suzuki
Masashi Ukai
Akiyoshi Ohtake
Original Assignee
Astellas Pharma Inc.
Priority date (The priority date 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 date listed.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40591069&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20121078(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astellas Pharma Inc. filed Critical Astellas Pharma Inc.
Publication of HRP20121078T1 publication Critical patent/HRP20121078T1/hr

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • 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.
HRP20121078AT 2007-11-02 2012-12-28 Farmaceutski sastav za lijeäśenje hiperaktivnog mjehura HRP20121078T1 (hr)

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

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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)

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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)

* Cited by examiner, † Cited by third party
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

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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