Viewing Study NCT00277238



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Last Modification Date: 2024-10-26 @ 9:22 AM
Study NCT ID: NCT00277238
Status: COMPLETED
Last Update Posted: 2017-03-08
First Post: 2006-01-13

Brief Title: CPG10101 Combination Therapy For The Treatment Of Hepatitis C In Non-Responder Null And Partial Responder Hepatitis C Virus HCV Genotype 1 Infected Subjects
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: CPG 10101 Combination Therapy for the Treatment of Hepatitis C A Phase II Randomized Open Label Multi-Center Parallel Arm Controlled Trial of CPG 10101 at Two Different Dose Levels With Pegylated-Interferon-Alpha 2B PEG-IFN Plus Ribavirin RBV or PEG-IFN Plus RBV Without CPG 10101 in the Treatment of Non-Responder Null and Partial Responder HCV Genotype 1 Infected Subjects
Status: COMPLETED
Status Verified Date: 2017-03
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: The purpose of this study is to determine the efficacy and tolerability of CPG 10101 at two different dose levels with pegylated-interferon-alpha 2B PEG-IFN plus ribavirin RBV compared to PEG-IFN and RBV without CPG 10101 in HCV positive subjects who were classified as non-responders to previous adequate PEG-IFN plus RBV therapy
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
CPG 10101-004 None None None