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NCT00142103 · ClinicalTrials.gov registry record · Phase 1

CPG10101 Combination Therapy For The Treatment Of Hepatitis C In Relapsed Hepatitis C Virus (HCV) Subjects

A Phase 1 study, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
91
Enrollment target

NCT00142103 is a Phase 1 study that has completed, run by Pfizer. The registered enrollment target is 91 participants.

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The verdict

NCT00142103, a Phase 1 study, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
91 participants
Enrollment target

Study Summary

1. To characterize the tolerability profile of subcutaneous (SC) CPG 10101 alone, with pegylated interferon, ribavirin or both pegylated interferon and ribavirin when administered weekly for twelve weeks in relapsed HCV positive subjects. 2. To assess the effect of subcutaneous (SC) CPG 10101 alone, with pegylated interferon, ribavirin or both pegylated interferon and ribavirin on serum Hepatitis C Virus (HCV) RNA concentrations

Interventions

  • DRUG Control
  • DRUG CPG10101

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2005-09
Est. Completion 2007-02
Phase Phase 1

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT00142103

The ClinicalTrials.gov registry entry for NCT00142103 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

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

NCT00142103 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00142103 about?

NCT00142103 is a clinical study titled "CPG10101 Combination Therapy For The Treatment Of Hepatitis C In Relapsed Hepatitis C Virus (HCV) Subjects". 1. To characterize the tolerability profile of subcutaneous (SC) CPG 10101 alone, with pegylated interferon, ribavirin or both pegylated interferon and ribavirin when administered weekly for twelve weeks in relapsed HCV positive subjects. 2. To assess the effect of subcutaneous (SC) CPG 10101 alone,...

What is the current status of trial NCT00142103?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 91 participants. The study started on 2005-09. Estimated completion is 2007-02.

What interventions are being tested in trial NCT00142103?

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

Who is sponsoring clinical trial NCT00142103?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.