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Generated: November 23, 2017

DrugPatentWatch Database Preview

Claims for Patent: 4,771,041

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Claims for Patent: 4,771,041

Title: Method for combating virus infection
Abstract:A method for the selective treatment of virus infections in animals and man comprising administering to a host so infected a therapeutically effective amount of phosphonoformic acid or a physiologically acceptable salt thereof.
Inventor(s): Eriksson; Bertil F. H. (Tumba, SE), Helgstrand; Ake J. E. (Lund, SE), Misiorny, deceased; Alfons (late of Bandhagen, SE), Misiorny, legal representive; Karl H. (Sodertalje, SE), Stening; Goran B. (Sodertalje, SE), Stridh; Stig-Ake A. (Sodertalje, SE)
Assignee: Astra Lakemedel Aktiebolag (SE)
Application Number:06/793,575
Patent Claims: 1. A method for the treatment of virus-induced diseases in animals including man, by inhibiting transformation of virus-infected cells, characterized by administering to an animal so infected an amount of phosphonoformic acid or a physiological salt thereof effective to inhibit the transformation of said virus-infected cells.

2. A method according to claim 1, wherein the infected animal is treated with the tri-sodium salt of phosphonoformic acid.

3. A method according to claim 2 wherein the tri-sodium salt of phosphonoformic acid is orally administered.

4. A method according to claim 1 wherein the phosphonoformic acid or physiologically effective salt thereof is orally administered.

5. A method for inhibiting the replication of a retrovirus in animals including man, comprising administering to an animal in need of such treatment phosphonoformic acid or a physiologically acceptable salt thereof in an amount sufficient for inhibiting said replication.

6. A method according to claim 5 wherein the phosphonoformic acid or physiologically effective salt thereof is orally administered.

7. A pharmaceutical composition effective for treating virus infections or diseases in animals and man suitable for oral administration to humans comprising as an active ingredient phosphonoformic acid or a physiologically acceptable salt thereof in an amount effective to inhibit replication of the virus or multiplication of a virus-transformed cell, together with a pharmaceutically acceptable carrier free of pharmaceutically unacceptable impurities and suitable for oral administration to humans.

8. A pharmaceutical composition according to claim 7 in which the active ingredient comprises about 0.1% to about 50% of the preparation.
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Cipla
Accenture
Healthtrust
Boehringer Ingelheim
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Chubb
Citi
AstraZeneca

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