RU2002102076A - PHARMACEUTICAL COMPOSITION CONTAINING SIBUTRAMINE AND ORLISTAT - Google Patents

PHARMACEUTICAL COMPOSITION CONTAINING SIBUTRAMINE AND ORLISTAT

Info

Publication number
RU2002102076A
RU2002102076A RU2002102076/14A RU2002102076A RU2002102076A RU 2002102076 A RU2002102076 A RU 2002102076A RU 2002102076/14 A RU2002102076/14 A RU 2002102076/14A RU 2002102076 A RU2002102076 A RU 2002102076A RU 2002102076 A RU2002102076 A RU 2002102076A
Authority
RU
Russia
Prior art keywords
formula
compound
pharmaceutically acceptable
enantiomers
methyl
Prior art date
Application number
RU2002102076/14A
Other languages
Russian (ru)
Other versions
RU2229289C2 (en
Inventor
Дэвид Джон ХИЛ
Original Assignee
Кнолль Гмбх
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
Priority claimed from GBGB9914744.9A external-priority patent/GB9914744D0/en
Application filed by Кнолль Гмбх filed Critical Кнолль Гмбх
Publication of RU2002102076A publication Critical patent/RU2002102076A/en
Application granted granted Critical
Publication of RU2229289C2 publication Critical patent/RU2229289C2/en

Links

Claims (8)

1. Способ лечения сопутствующих патологических состояний, связанных с ожирением, у человека, нуждающегося в таком лечении, который включает назначение этому человеку эффективного с терапевтической точки зрения количества соединения формулы I1. A method of treating concomitant pathological conditions associated with obesity in a person in need of such treatment, which comprises administering to that person a therapeutic effective amount of a compound of formula I
Figure 00000001
Figure 00000001
включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, и эффективного с терапевтической точки зрения количества соединения формулы IIincluding its enantiomers and pharmaceutically acceptable salts in which R 1 and R 2 are independently H or methyl, and a therapeutically effective amount of a compound of formula II
Figure 00000002
Figure 00000002
причем соединение формулы I и соединение формулы II принимаются одновременно, по отдельности или последовательно.moreover, the compound of formula I and the compound of formula II are taken simultaneously, individually or sequentially.
2. Способ по п.1, отличающийся тем, что соединение формулы I представляет собой
Figure 00000003
-{1-[1-(4-хлорфенил)-циклобутил]-3-метилбутил}-
Figure 00000004
-диметиламин или его соль.
2. The method according to claim 1, characterized in that the compound of formula I is a
Figure 00000003
- {1- [1- (4-chlorophenyl) cyclobutyl] -3-methylbutyl} -
Figure 00000004
dimethylamine or its salt.
3. Способ по п.2, отличающийся тем, что соединение формулы I принимается в период от 30 мин до 3 ч до приема соединения формулы II.3. The method according to claim 2, characterized in that the compound of formula I is taken in the period from 30 minutes to 3 hours before receiving the compounds of formula II. 4. Соединение формулы I, включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, и соединение формулы II, предназначенные для лечения сопутствующих патологических состояний, связанных с ожирением, путем приема, выполняемого одновременно, по отдельности или последовательно.4. The compound of formula I, including its enantiomers and pharmaceutically acceptable salts, in which R 1 and R 2 independently mean H or methyl, and the compound of formula II, intended for the treatment of concomitant pathological conditions associated with obesity, by administration performed simultaneously, individually or sequentially. 5. Соединение формулы I, включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, и соединение формулы II в качестве комбинированного препарата, предназначенного для лечения сопутствующих патологических состояний, связанных с ожирением, путем приема, выполняемого одновременно, по отдельности или последовательно.5. The compound of formula I, including its enantiomers and pharmaceutically acceptable salts, in which R 1 and R 2 independently mean H or methyl, and the compound of formula II as a combined preparation for the treatment of concomitant pathological conditions associated with obesity, by reception performed simultaneously, individually or sequentially. 6. Продукт, содержащий соединение формулы I, включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, и соединение формулы II в качестве комбинированного препарата, предназначенного для лечения сопутствующих патологических состояний, связанных с ожирением, путем приема, выполняемого одновременно, по отдельности или последовательно.6. A product containing a compound of formula I, including its enantiomers and pharmaceutically acceptable salts, in which R 1 and R 2 are independently H or methyl, and a compound of formula II as a combination preparation for the treatment of concomitant pathological conditions associated with obesity, by admission performed simultaneously, individually or sequentially. 7. Применение продукта, содержащего соединение формулы I, включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, для изготовления лекарственного препарата, предназначенного для лечения сопутствующих патологических состояний, связанных с ожирением, у пациента, который также получает лечение с помощью орлистата.7. The use of a product containing a compound of formula I, including its enantiomers and pharmaceutically acceptable salts, in which R 1 and R 2 are independently H or methyl, for the manufacture of a medicament for the treatment of concomitant pathological conditions associated with obesity, in a patient who is also receiving treatment with orlistat. 8. Фармацевтическая композиция, включающая соединение формулы I8. A pharmaceutical composition comprising a compound of formula I
Figure 00000005
Figure 00000005
включая его энантиомеры и приемлемые с фармацевтической точки зрения соли, в которых R1 и R2 независимо означают Н или метил, и соединение формулы IIincluding its enantiomers and pharmaceutically acceptable salts, in which R 1 and R 2 independently mean H or methyl, and a compound of formula II
Figure 00000006
Figure 00000006
совместно с приемлемым с фармацевтической точки зрения разбавителем или носителем.together with a pharmaceutically acceptable diluent or carrier.
RU2002102076/14A 1999-06-24 2000-06-16 Pharmaceutical composition containing sibutramine and orlistat RU2229289C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9914744.9 1999-06-24
GBGB9914744.9A GB9914744D0 (en) 1999-06-24 1999-06-24 Therapeutic agents

Publications (2)

Publication Number Publication Date
RU2002102076A true RU2002102076A (en) 2003-09-20
RU2229289C2 RU2229289C2 (en) 2004-05-27

Family

ID=10855955

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2002102076/14A RU2229289C2 (en) 1999-06-24 2000-06-16 Pharmaceutical composition containing sibutramine and orlistat

Country Status (21)

Country Link
EP (1) EP1187606A1 (en)
JP (1) JP2003503349A (en)
KR (1) KR20020015357A (en)
CN (1) CN1358092A (en)
AU (1) AU5533200A (en)
BG (1) BG106180A (en)
BR (1) BR0011880A (en)
CA (1) CA2375972A1 (en)
CZ (1) CZ20014613A3 (en)
GB (1) GB9914744D0 (en)
HK (1) HK1049278A1 (en)
HU (1) HUP0201878A3 (en)
IL (1) IL147079A0 (en)
MX (1) MXPA01012936A (en)
NO (1) NO20016224L (en)
PL (1) PL352402A1 (en)
RU (1) RU2229289C2 (en)
SK (1) SK18242001A3 (en)
TR (1) TR200103699T2 (en)
WO (1) WO2001000205A1 (en)
ZA (1) ZA200109989B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6696495B2 (en) * 1998-12-02 2004-02-24 Snowden Pharmaceuticals, Llc Treatment of disorders secondary to organic impairments
US20040214804A1 (en) * 2003-04-25 2004-10-28 Pharmacia Corporation Combination of an aldosterone receptor antagonist and an anti-obesity agent
AU2005298692A1 (en) 2004-10-25 2006-05-04 Solvay Pharmaceuticals Gmbh Pharmaceutical compositions comprising CB1 cannabinoid receptor antagonists and potassium channel openers for the treatment of diabetes mellitus type I, obesity and related conditions
EP2066329B1 (en) 2006-09-15 2017-09-06 Reviva Pharmaceuticals, Inc. Synthesis, methods of using, and compositions of cyclobutylmethylamines
US8604244B2 (en) 2010-07-02 2013-12-10 Reviva Pharmaceuticals, Inc. Compositions, synthesis, and methods of using cycloalkylmethylamine derivatives
KR20080046601A (en) * 2006-11-22 2008-05-27 에스케이케미칼주식회사 Inclusion complex of sibutramine and beta-cyclodextrin
CN101890017A (en) * 2009-05-22 2010-11-24 北京奥萨医药研究中心有限公司 Medicament composition containing sibutramine and stanin fat-reducing medicament and application thereof
MX336980B (en) 2010-12-21 2016-02-09 Senosiain S A De C V Lab Combination and composition for treating obesity.
WO2013102195A1 (en) 2011-12-30 2013-07-04 Reviva Pharmaceuticals, Inc. Compositions, synthesis, and methods of using phenylcycloalkylmethylamine derivatives

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9727131D0 (en) * 1997-12-24 1998-02-25 Knoll Ag Therapeutic agents

Similar Documents

Publication Publication Date Title
JP2020507589A5 (en)
JP2008510758A5 (en)
JP2006523216A5 (en)
US11351191B2 (en) Silicate containing compositions and methods of treatment
RU2004110055A (en) NEW DIPEPTIDYL PEPTIDASE IV INHIBITORS AS ANTI-DIABETIC AGENTS
EP2036902A3 (en) Urea compounds active as vanilloid receptor antagonist for the treatment of pain
LU90956I2 (en) Metvix active ingredient methylaminolevulinic in the form of a salt preferably methylaminolevulinic hydrochloride
RU97115713A (en) COMPOUNDS CONTAINING PETROPYRANES AND METHOD OF APPLICATION
JP2005506352A5 (en)
RU94045155A (en) Methods of alzheimer's disease inhibition
RU2004136853A (en) (S) -4-amino-5-chloro-2-methoxy-n- [1- [1- (2-tetrahydrofurylcarbonyl) -4-piperidini-methyl] -4-piperidinyl] benzamide, method of obtaining it, commercially AND INTERMEDIATE CONNECTION FOR ITS PRODUCTION
RU2007140701A (en) APOMORPHINE PHARMACEUTICAL COMPOSITION FOR TRANSBUKCAL INTRODUCTION
JP2019515908A5 (en)
JP2006514092A5 (en)
RU2002102076A (en) PHARMACEUTICAL COMPOSITION CONTAINING SIBUTRAMINE AND ORLISTAT
JP2011518168A5 (en)
RU2002101622A (en) Naphthoquinone derivatives and their use for the treatment and control of tuberculosis
RU2003130644A (en) RARCARBOLINE DERIVATIVES AND THEIR PHARMACEUTICAL USE AGAINST DIPRESSION AND FEAR
RU2002128917A (en) Polyamine analogues as cytotoxic agents
RU2005133665A (en) APPLICATION OF 10-HYDROXY-10,11-DIHYDROCARBAMAZEPINE DERIVATIVES FOR THE TREATMENT OF AFFECTIVE DISORDERS
JPH0325407B2 (en)
RU2002118700A (en) SUBSTITUTED DERIVATIVES OF NORBORNILAMINE, METHOD FOR PRODUCING THEM, THEIR USE AS MEDICINES OR DIAGNOSTIC MEDICINES, AND ALSO CONTAINING THEIR MEDICINES
RU2004131214A (en) METHODS FOR TREATING COGNITIVE DISORDERS
WO2005014032A3 (en) Use of secretagogues like ghrelin in cancer cachexia and for stimulating appetite
EA006295B1 (en) Use of distamycin derivatives for antitumor therapy