Clinical trial

A Study Evaluating the Safety and Clinical Activity of HCV-796 in…

NCT00367887 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00367887
Title A Study Evaluating the Safety and Clinical Activity of HCV-796 in Treatment-Naive and Non-Responder Subjects
Official title A Phase 2, Randomized, Open-Label Study Of The Safety, Antiviral Activity, And Pharmacokinetics Of HCV-796 Administered In Combination With Peginterferon Alfa 2B (Peg-Intron) Plus Ribavirin (Rebetol) Versus Peg-Intron Plus Rebetol In Subjects With Hepatitis C Virus Genotype 1 Infection
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Collaborators ViroPharma Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Hepatitis C
Intervention type Drug
Interventions Peg-Intron, REBETOL, HCV 796
Enrollment 246
Start date Oct 1, 2006
Primary completion Jul 1, 2008
Completion Jul 1, 2008
First posted Aug 23, 2006
Last update posted Feb 11, 2013
Countries Puerto Rico, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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