EA200870430A1 - INTRAMUSCULAR ANTIVIRUS METHODS OF TREATMENT - Google Patents

INTRAMUSCULAR ANTIVIRUS METHODS OF TREATMENT

Info

Publication number
EA200870430A1
EA200870430A1 EA200870430A EA200870430A EA200870430A1 EA 200870430 A1 EA200870430 A1 EA 200870430A1 EA 200870430 A EA200870430 A EA 200870430A EA 200870430 A EA200870430 A EA 200870430A EA 200870430 A1 EA200870430 A1 EA 200870430A1
Authority
EA
Eurasian Patent Office
Prior art keywords
iii
compound
formula
pharmaceutically acceptable
acceptable salt
Prior art date
Application number
EA200870430A
Other languages
Russian (ru)
Inventor
Ярлагадда С. Бабу
Пооран Чанд
Шанта Бантиа
Шейн Арнольд
Джон Майкл Килпатрик
Original Assignee
Байокрист Фармасьютикалз, Инк.
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 Байокрист Фармасьютикалз, Инк. filed Critical Байокрист Фармасьютикалз, Инк.
Publication of EA200870430A1 publication Critical patent/EA200870430A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/16Antivirals for RNA viruses for influenza or rhinoviruses
    • 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

Abstract

Изобретение обеспечивает способ лечения вирусной инфекции у человека, включающий введение эффективного количества соединения формулы I, II, III или IVили его фармацевтически приемлемой соли. Изобретение включает также способ ингибирования нейраминидазы у человека, предусматривающий введение эффективного количества соединения формулы I, II, III или IV или его фармацевтически приемлемой соли. Изобретение обеспечивает стандартную лекарственную форму, содержащую приблизительно до 500 мг соединения формулы I, II, III или IV или его фармацевтически приемлемой соли, и набор, содержащий соединение формулы I, II, III или IV или его фармацевтически приемлемую соль, и инструкции для введения этого соединения человеку внутримышечным путем. Изобретение обеспечивает применение соединения формулы I, II, III или IV или его фармацевтически приемлемой соли для увеличения продолжительности жизни и/или уменьшения смертности в группе млекопитающих подвергнутых воздействию источника вируса гриппа.The invention provides a method of treating a viral infection in humans, comprising administering an effective amount of a compound of formula I, II, III or IV, or a pharmaceutically acceptable salt thereof. The invention also includes a method of inhibiting neuraminidase in humans, comprising administering an effective amount of a compound of formula I, II, III or IV, or a pharmaceutically acceptable salt thereof. The invention provides a unit dosage form containing up to about 500 mg of a compound of formula I, II, III or IV, or a pharmaceutically acceptable salt thereof, and a kit containing a compound of formula I, II, III or IV, or a pharmaceutically acceptable salt thereof, and instructions for administering this connections to a person intramuscularly. The invention provides the use of a compound of formula I, II, III or IV, or a pharmaceutically acceptable salt thereof, to increase life expectancy and / or decrease mortality in a group of mammals exposed to a source of influenza virus.

EA200870430A 2006-04-12 2006-04-12 INTRAMUSCULAR ANTIVIRUS METHODS OF TREATMENT EA200870430A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2006/013535 WO2007117241A1 (en) 2006-04-12 2006-04-12 Intramuscular antiviral treatments

Publications (1)

Publication Number Publication Date
EA200870430A1 true EA200870430A1 (en) 2009-06-30

Family

ID=37671157

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200870430A EA200870430A1 (en) 2006-04-12 2006-04-12 INTRAMUSCULAR ANTIVIRUS METHODS OF TREATMENT

Country Status (8)

Country Link
JP (1) JP2009533428A (en)
CN (1) CN104784166A (en)
AU (1) AU2006341592A1 (en)
BR (1) BRPI0621552A2 (en)
CA (1) CA2649090A1 (en)
EA (1) EA200870430A1 (en)
MX (1) MX2008013140A (en)
WO (1) WO2007117241A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0518443D0 (en) 2005-09-09 2005-10-19 Evolutec Ltd Method of treating myasthenia gravis
CN101367750B (en) * 2007-08-14 2012-05-23 中国人民解放军军事医学科学院毒物药物研究所 (1S,2S,3S,4R)-3-[(1S)-1-acet-ammonia-2-ethyl-butyl]-4- guanidino-2-hydroxyl-cyclopentyl-1-carboxylic acid aqua compound and medical uses thereof
JP5840623B2 (en) * 2010-01-08 2016-01-06 ヴォリューション イミュノ ファーマシューティカルズ エスエイ EV576 for use in the treatment of respiratory tract viral infections
CN102584637B (en) * 2011-01-17 2014-07-09 天津药物研究院 Peramivir hydrate crystal, preparation method, medical compound and usage thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1040094T1 (en) * 1997-12-17 2009-10-31 Biocryst Pharm Inc Substituted cyclopentane and cyclopentene compounds useful as neuraminidase inhibitors
GB0015324D0 (en) * 2000-06-22 2000-08-16 Biota Scient Management Medicaments

Also Published As

Publication number Publication date
MX2008013140A (en) 2009-02-12
BRPI0621552A2 (en) 2011-12-13
WO2007117241A1 (en) 2007-10-18
AU2006341592A1 (en) 2007-10-18
CN104784166A (en) 2015-07-22
JP2009533428A (en) 2009-09-17
CA2649090A1 (en) 2007-10-18

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