RU2000103216A - NEW COMPOSITION - Google Patents

NEW COMPOSITION

Info

Publication number
RU2000103216A
RU2000103216A RU2000103216/14A RU2000103216A RU2000103216A RU 2000103216 A RU2000103216 A RU 2000103216A RU 2000103216/14 A RU2000103216/14 A RU 2000103216/14A RU 2000103216 A RU2000103216 A RU 2000103216A RU 2000103216 A RU2000103216 A RU 2000103216A
Authority
RU
Russia
Prior art keywords
pharmaceutical composition
composition according
paragraphs
drying
halogen
Prior art date
Application number
RU2000103216/14A
Other languages
Russian (ru)
Other versions
RU2216330C2 (en
Inventor
Джоанн БРОДХЕД
Original Assignee
Астра Фармасьютикалз Лтд.
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 SE9702680A external-priority patent/SE9702680D0/en
Application filed by Астра Фармасьютикалз Лтд. filed Critical Астра Фармасьютикалз Лтд.
Publication of RU2000103216A publication Critical patent/RU2000103216A/en
Application granted granted Critical
Publication of RU2216330C2 publication Critical patent/RU2216330C2/en

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Claims (10)

1. Фармацевтическая композиция, содержащая нуклеотидный аналог и одну или несколько стеклообразующих добавок.1. A pharmaceutical composition comprising a nucleotide analogue and one or more glass-forming additives. 2. Фармацевтическая композиция по п. 1, где нуклеотид является соединением формулы (I)
Figure 00000001

где R1 и R2 независимо обозначают водород или галоген, R3 и R4 независимо обозначают фенил или С1-6-алкил, необязательно замещенный одним или несколькими заместителями, выбранными из OR5, С1-6-алкилтио, NR6R7, фенила, COOR8 и галогена, R5, R6, R7 и R8 независимо обозначают водород или С1-6-алкил и Х обозначает кислотную часть молекулы, или его фармацевтически приемлемой солью.
2. The pharmaceutical composition according to claim 1, wherein the nucleotide is a compound of formula (I)
Figure 00000001

where R 1 and R 2 independently represent hydrogen or halogen, R 3 and R 4 independently represent phenyl or C 1-6 alkyl optionally substituted with one or more substituents selected from OR 5 , C 1-6 alkylthio, NR 6 R 7 , phenyl, COOR 8 and halogen, R 5 , R 6 , R 7 and R 8 are independently hydrogen or C 1-6 alkyl and X is the acid part of the molecule, or a pharmaceutically acceptable salt thereof.
3. Фармацевтическая композиция по п. 1 или 2, которая находится в лиофилизованной, высушенной распылительной сушкой или высушенной в вакууме форме. 3. The pharmaceutical composition according to claim 1 or 2, which is in a lyophilized, spray dried, or vacuum dried form. 4. Фармацевтическая композиция по любому из пп. 1-3, которая находится в восстановленной форме. 4. The pharmaceutical composition according to any one of paragraphs. 1-3, which is in reduced form. 5. Фармацевтическая композиция по любому из пп. 1-3, в которой модифицирующим агентом является сахароза. 5. The pharmaceutical composition according to any one of paragraphs. 1-3, in which the modifying agent is sucrose. 6. Фармацевтическая композиция по любому из пп. 1-5 как лекарственное средство в терапии. 6. The pharmaceutical composition according to any one of paragraphs. 1-5 as a medicine in therapy. 7. Фармацевтическая композиция по любому из пп. 1-5 для лечения острых коронарных синдромов и для чрескожной внутрипросветной ангиопластики. 7. The pharmaceutical composition according to any one of paragraphs. 1-5 for the treatment of acute coronary syndromes and for percutaneous intraluminal angioplasty. 8. Фармацевтическая композиция по любому из пп. 1-5 для лечения стенокардии. 8. The pharmaceutical composition according to any one of paragraphs. 1-5 for the treatment of angina pectoris. 9. Способ лечения расстройства, связанного с агрегацией тромбоцитов, предусматривающий предоставление субъекту, страдающему от этого расстройства, терапевтически эффективного количества фармацевтической композиции, определенной в любом из пп. 1-5. 9. A method of treating a disorder associated with platelet aggregation, comprising providing a subject suffering from this disorder with a therapeutically effective amount of a pharmaceutical composition as defined in any one of claims. 1-5. 10. Способ приготовления фармацевтической композиции по п. 3, предусматривающий смешивание ингредиентов этой композиции и либо замораживание их и высушивание смеси, либо высушивание их распылительной сушкой. 10. The method of preparing the pharmaceutical composition according to claim 3, comprising mixing the ingredients of this composition and either freezing them and drying the mixture, or drying them by spray drying.
RU2000103216/14A 1997-07-11 1998-06-29 Nucleotide analog-containing pharmaceutical composition and method for it preparing RU2216330C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9702680A SE9702680D0 (en) 1997-07-11 1997-07-11 New formulation
SE9702680-1 1997-07-11

Publications (2)

Publication Number Publication Date
RU2000103216A true RU2000103216A (en) 2002-01-10
RU2216330C2 RU2216330C2 (en) 2003-11-20

Family

ID=20407718

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2000103216/14A RU2216330C2 (en) 1997-07-11 1998-06-29 Nucleotide analog-containing pharmaceutical composition and method for it preparing

Country Status (36)

Country Link
US (1) US6130208A (en)
EP (1) EP1000079B1 (en)
JP (1) JP4950380B2 (en)
KR (1) KR100786654B1 (en)
CN (2) CN1864696A (en)
AR (1) AR013157A1 (en)
AT (1) ATE340801T1 (en)
AU (1) AU8362598A (en)
BR (1) BR9810703A (en)
CA (1) CA2295628C (en)
CY (1) CY1105805T1 (en)
CZ (1) CZ298110B6 (en)
DE (1) DE69836023T2 (en)
DK (1) DK1000079T3 (en)
EE (1) EE04119B1 (en)
ES (1) ES2273425T3 (en)
HK (1) HK1026429A1 (en)
HU (1) HU226489B1 (en)
ID (1) ID24716A (en)
IL (2) IL133868A0 (en)
IS (1) IS2439B (en)
MY (1) MY116421A (en)
NO (1) NO329918B1 (en)
NZ (1) NZ502073A (en)
PL (1) PL192768B1 (en)
PT (1) PT1000079E (en)
RU (1) RU2216330C2 (en)
SA (1) SA98190328B1 (en)
SE (1) SE9702680D0 (en)
SI (1) SI1000079T1 (en)
SK (1) SK285766B6 (en)
TR (1) TR200000006T2 (en)
TW (1) TW585764B (en)
UA (1) UA65576C2 (en)
WO (1) WO1999002542A1 (en)
ZA (1) ZA985669B (en)

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US20120141468A1 (en) 2008-05-13 2012-06-07 Lisa Ruderman Chen Maintenance of platelet inhibition during antiplatelet therapy
US8759316B2 (en) 2008-05-13 2014-06-24 The Medicines Company Maintenance of platelet inhibition during antiplatelet therapy
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US9427448B2 (en) 2009-11-11 2016-08-30 The Medicines Company Methods of treating, reducing the incidence of, and/or preventing ischemic events
US9925265B2 (en) 2009-11-11 2018-03-27 Chiesi Farmaceutici S.P.A. Methods of treating or preventing stent thrombosis
US8729095B2 (en) 2009-08-28 2014-05-20 Daiichi Sankyo Company, Limited 3-(biaryloxy)propionic acid derivatives for prevention and/or treatment of thromboembolic diseases
US10376532B2 (en) 2009-11-11 2019-08-13 Chiesi Farmaceutici, S.P.A. Methods of treating, reducing the incidence of, and/or preventing ischemic events
MX2013006127A (en) * 2010-12-10 2013-09-26 Sigmapharm Lab Llc Highly stable compositions of orally active nucleotide analogues or orally active nucleotide analogue prodrugs.
CN103582480B (en) 2011-02-09 2016-03-16 医药公司 The method for the treatment of pulmonary hypertension
DK2744424T3 (en) 2011-08-17 2018-01-22 Samuel Shiber Adaptively rotating catheter to open clogged vessels in the body
ES2904256T3 (en) 2013-03-09 2022-04-04 Chiesi Farm Spa Methods to treat, reduce the incidence of, and/or prevent ischemic events
CN103772461A (en) * 2014-01-06 2014-05-07 南京正科制药有限公司 Cangrelor crystal form I
BR112017014996A2 (en) 2015-01-14 2018-03-20 Chiesi Farm Spa pharmaceutical formulations and sealed containers
WO2018234565A1 (en) 2017-06-23 2018-12-27 Chiesi Farmaceutici S.P.A. Method of preventing of systemic-to-pulmonary-artery shunt thrombosis
CN112469710B (en) 2018-06-19 2024-05-14 优时比制药有限公司 Pyridyl and pyrazinyl- (aza) indole sulfonamides

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KR0131678B1 (en) * 1991-12-09 1998-04-17 유미꾸라 레이이찌 Stabilized parathyroid hormone composition
DE69406649T2 (en) * 1993-02-10 1998-03-05 Astra Pharmaceuticals Ltd., Kings Langley, Hertfordshire N-ALKYL-2 SUBSTITUTED ATP ANALOGS
RU2135176C1 (en) * 1993-12-14 1999-08-27 Эли Лилли Энд Компани Water-dissolved inclusion complex of benzothiophene compounds with water-soluble cyclodextrin, method of synthesis and pharmaceutical composition
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