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NCT00277238 · ClinicalTrials.gov registry record · Phase 2

CPG10101 Combination Therapy For The Treatment Of Hepatitis C In Non-Responder (Null And Partial Responder) Hepatitis C Virus (HCV) Genotype 1 Infected Subjects

A Phase 2 study, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
113
Enrollment target

NCT00277238: Completed Phase 2 study, sponsored by Pfizer.

NCT00277238 is a Phase 2 study that has completed, run by Pfizer. The registered enrollment target is 113 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00277238, a Phase 2 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
113 participants
Enrollment target

Study 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.

Interventions

  • DRUG Control
  • DRUG CPG10101

Trial Details

FieldValue
Enrollment Target 113 participants
Start Date 2006-02
Est. Completion 2007-07
Phase Phase 2
Pfizer

1,845 total trials

What the finished NCT00277238 record still lists

NCT00277238 is an interventional study that assigns participants to a tested intervention. The registered 113 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (15% lower).

The record links to 0 conditions, and to 2 interventions - of which Control is the first listed.

NCT00277238 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00277238 about?

NCT00277238 is a clinical study titled "CPG10101 Combination Therapy For The Treatment Of Hepatitis C In Non-Responder (Null And Partial Responder) Hepatitis C Virus (HCV) Genotype 1 Infected Subjects". 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...

What is the current status of trial NCT00277238?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 113 participants. The study started on 2006-02. Estimated completion is 2007-07.

What interventions are being tested in trial NCT00277238?

The interventions under investigation include: Control (DRUG), CPG10101 (DRUG).

Who is sponsoring clinical trial NCT00277238?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00277238's enrollment target sits among peer trials

113 631st of 2000 higher than 1,370 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00277238, the US trial registry maintained by the National Library of Medicine. NCT00277238 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.