CL2014001397A1 -
Pharmaceutical composition comprising a) gs-7977 and b) at least one pharmaceutically stable excipient; unit dosage form; composition preparation process; use of the composition to treat an infection caused by the hepatitis c virus.
- Google Patents
Pharmaceutical composition comprising a) gs-7977 and b) at least one pharmaceutically stable excipient; unit dosage form; composition preparation process; use of the composition to treat an infection caused by the hepatitis c virus.
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Family has litigation
First worldwide family litigation filedlitigationCriticalhttps://patents.darts-ip.com/?family=52002386&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CL2014001397(A1)"Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US13/661,509external-prioritypatent/US20130109647A1/en
Application filed by Gilead Pharmasset LlcfiledCriticalGilead Pharmasset Llc
Publication of CL2014001397A1publicationCriticalpatent/CL2014001397A1/en
CL2014001397A2011-11-292014-05-27
Pharmaceutical composition comprising a) gs-7977 and b) at least one pharmaceutically stable excipient; unit dosage form; composition preparation process; use of the composition to treat an infection caused by the hepatitis c virus.
CL2014001397A1
(en)
Pharmaceutical composition comprising a) gs-7977 and b) at least one pharmaceutically stable excipient; unit dosage form; composition preparation process; use of the composition to treat an infection caused by the hepatitis c virus.
Condensed tricyclic compounds and their pharmaceutically acceptable salts; pharmaceutical composition that includes them; and its use in the treatment of a viral infection.
Compounds derived from substituted nucleosides, nucleotides and analogs thereof; pharmaceutical composition; and use to improve or treat a viral infection.
Tenofovir Alafenamide Hemifumarate; Preparation method; pharmaceutical composition that includes it; method to prepare the pharmaceutical composition; and use in the treatment of a hiv infection.
Compounds derived from imidazo [1,2-f] [1,2,4] triazinyl nucleosides; pharmaceutical composition that includes them; and its use for the treatment of a flaviviridae virus infection, particularly hepatitis c virus infections.
Compounds derived from 5-ethynyl-3 (formylamino) thiophene-2-carboxylic acid, inhibitors of viruses of the flaviviridae family; pharmaceutical composition comprising a compound; and their use of the compounds in the preparation of drugs.
Compounds derived from thiophene-2-carboxylic acid, flaviviridae virus inhibitors; pharmaceutical composition that includes them; and its use for the treatment of a viral infection by flaviviridae.
Compounds derived from nucleosides, nucleotides and analogs thereof; pharmaceutical composition; and its use to prepare a useful medicine in the treatment of hepatitis c.
Compounds derived from nitrogen heterocycles, inhibitors of influenza virus replication; Preparation method; pharmaceutical composition; method to inhibit influenza virus replication in a biological sample or a patient.
Compounds derived from pyrazolo [1,5-a] pyrimidines or a pharmaceutically acceptable salt thereof; pharmaceutical composition that includes them; and its use to treat a pneumovirinae virus infection or a respiratory syncytial virus infection.
Capsule formulation comprising at least one compound of formula (i), solubilized; method of administration of the formulation; use to treat a hepatitis c virus infection.
compound, pharmaceutical composition, use of the compound or a pharmaceutically acceptable salt thereof, and method of treating an hcv infected patient