WO2008147245A3 - Controlled release proxodolol pharmaceutical composition - Google Patents

Controlled release proxodolol pharmaceutical composition Download PDF

Info

Publication number
WO2008147245A3
WO2008147245A3 PCT/RU2007/000619 RU2007000619W WO2008147245A3 WO 2008147245 A3 WO2008147245 A3 WO 2008147245A3 RU 2007000619 W RU2007000619 W RU 2007000619W WO 2008147245 A3 WO2008147245 A3 WO 2008147245A3
Authority
WO
WIPO (PCT)
Prior art keywords
proxodolol
controlled release
pharmaceutically acceptable
active ingredient
pharmaceutical composition
Prior art date
Application number
PCT/RU2007/000619
Other languages
French (fr)
Russian (ru)
Other versions
WO2008147245A2 (en
Inventor
Sergei Danilovich Juzhakov
Robert Georgievich Glushkov
Viktor Vladimirovich Chistyakov
Natalya Vyacheslavovna Aristovskaya
Original Assignee
Otkrytoe Aktsionernoe Obschest
Sergei Danilovich Juzhakov
Robert Georgievich Glushkov
Chistyakov Viktor Vladimirovic
Aristovskaya Natalya Vyachesla
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.)
Filing date
Publication date
Application filed by Otkrytoe Aktsionernoe Obschest, Sergei Danilovich Juzhakov, Robert Georgievich Glushkov, Chistyakov Viktor Vladimirovic, Aristovskaya Natalya Vyachesla filed Critical Otkrytoe Aktsionernoe Obschest
Publication of WO2008147245A2 publication Critical patent/WO2008147245A2/en
Publication of WO2008147245A3 publication Critical patent/WO2008147245A3/en

Links

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
    • A61K31/41Heterocyclic 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
    • A61K31/4245Oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

The invention relates to medicine, in particular to pharmaceutic. A novel preparation exhibiting stable kinetic characteristics relating to delivery of an active substance is disclosed. The controlled release proxodolol pharmaceutical forms can be effectively and easily produced using a mixture of one or more expanding or gel-forming components, an active ingredient and a pharmaceutically acceptable filler. In the preferred embodiment, a preparation in the form of tablets containing proxodolol in a quantity of 120 mg, hypromellose and pharmaceutically acceptable fillers, for example microcristalline cellulose, calcium stearate and aerosil, is used. The novel pharmaceutical forms with a suitable proxodolol release make it possible to reduce the number of every day medications, whilst the concentration of the active ingredient remains constant within a therapeutic dose.
PCT/RU2007/000619 2007-06-01 2007-11-13 Controlled release proxodolol pharmaceutical composition WO2008147245A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
RU2007120431/15A RU2356532C2 (en) 2007-06-01 2007-06-01 Controlled-release pharmaceutical proxodolol composition
RU2007120431 2007-06-01

Publications (2)

Publication Number Publication Date
WO2008147245A2 WO2008147245A2 (en) 2008-12-04
WO2008147245A3 true WO2008147245A3 (en) 2009-06-04

Family

ID=40075688

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/RU2007/000619 WO2008147245A2 (en) 2007-06-01 2007-11-13 Controlled release proxodolol pharmaceutical composition

Country Status (2)

Country Link
RU (1) RU2356532C2 (en)
WO (1) WO2008147245A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103477224B (en) * 2011-03-04 2015-12-23 贝克顿·迪金森公司 Blood collection device containing lysophosphatide enzyme inhibitor

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996014070A1 (en) * 1994-11-02 1996-05-17 Janssen Pharmaceutica N.V. Cisapride extended release oral compositions
WO2000021525A2 (en) * 1998-10-14 2000-04-20 Novartis Ag Sustained release pharmaceutical composition and method of releasing pharmaceutically active agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996014070A1 (en) * 1994-11-02 1996-05-17 Janssen Pharmaceutica N.V. Cisapride extended release oral compositions
WO2000021525A2 (en) * 1998-10-14 2000-04-20 Novartis Ag Sustained release pharmaceutical composition and method of releasing pharmaceutically active agent

Also Published As

Publication number Publication date
RU2007120431A (en) 2008-12-10
WO2008147245A2 (en) 2008-12-04
RU2356532C2 (en) 2009-05-27

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