Viewing Study NCT00367887



Ignite Creation Date: 2024-05-05 @ 5:01 PM
Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00367887
Status: COMPLETED
Last Update Posted: 2013-02-11
First Post: 2006-08-21

Brief Title: A Study Evaluating the Safety and Clinical Activity of HCV-796 in Treatment-Naive and Non-Responder Subjects
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

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
Status: COMPLETED
Status Verified Date: 2013-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a phase 2 randomized open-label study comparing the safety antiviral activity and pharmacokinetics of HCV-796 administered in combination with peginterferon alfa 2B Peg-Intron plus concomitant Rebetol vs Peg-Intron plus Rebetol in Hepatitis C Virus HCV genotype

1-infected subjects who are either naive to treatment or who have previously failed treatment non-responders
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
B3381001 None None None