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NCT00911963 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics of Multiple Ascending Doses of VCH-222 in Subjects With Chronic Hepatitis C Infection

A Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.

Completed
Registry status
Phase 1
Development phase
49
Enrollment target

NCT00911963 is a Phase 1 study that has completed, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 49 participants.

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The verdict

NCT00911963, a Phase 1 study, has completed, sponsored by Vertex Pharmaceuticals Incorporated.

COMPLETED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

The purpose of this study is to assess antiviral activity when administered alone for 3 days or in combination with peginterferon and ribavirin for 12 weeks. This study will also evaluate the safety and tolerability of treatment with VCH-222 when given alone or in combination with peginterferon and ribavirin. The study will also evaluate the pharmacokinetic profile of VCH-222 in HCV infected subjects.

Interventions

  • DRUG ribavirin
  • BIOLOGICAL peginterferon alfa-2a
  • DRUG VCH-222 or matching placebo

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2009-04
Est. Completion 2012-09
Phase Phase 1

Sponsor

Vertex Pharmaceuticals Incorporated

191 total trials

What the Registry Record Tells You About NCT00911963

The ClinicalTrials.gov registry entry for NCT00911963 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 49 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vertex Pharmaceuticals Incorporated, which has 191 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which ribavirin is the first listed.

NCT00911963 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00911963 about?

NCT00911963 is a clinical study titled "Pharmacokinetics of Multiple Ascending Doses of VCH-222 in Subjects With Chronic Hepatitis C Infection". The purpose of this study is to assess antiviral activity when administered alone for 3 days or in combination with peginterferon and ribavirin for 12 weeks. This study will also evaluate the safety and tolerability of treatment with VCH-222 when given alone or in combination with peginterferon and ...

What is the current status of trial NCT00911963?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2009-04. Estimated completion is 2012-09.

What interventions are being tested in trial NCT00911963?

The interventions under investigation include: ribavirin (DRUG), peginterferon alfa-2a (BIOLOGICAL), VCH-222 or matching placebo (DRUG).

Who is sponsoring clinical trial NCT00911963?

This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 191 total clinical trials registered on ClinicalTrials.gov.

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

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.