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NCT01467505 · ClinicalTrials.gov registry record · Phase 2

An Open Label Study of the Effect of Telaprevir in Combination With Ribavirin and Peginterferon on HCV Infection in Stable Liver Transplant Patients

A Phase 2 study, sponsored by Vertex Pharmaceuticals Incorporated.

Terminated
Registry status
Phase 2
Development phase
61
Enrollment target

NCT01467505 is a Phase 2 study that was terminated before completion, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 61 participants.

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The verdict

NCT01467505, a Phase 2 study, was terminated before completion, sponsored by Vertex Pharmaceuticals Incorporated.

TERMINATED
Registry status
Phase 2
Development phase
61 participants
Enrollment target

Study Summary

To assess efficacy of telaprevir, pegylated interferon alfa-2a (Peg-IFN-alfa-2a), and ribavirin (RBV) for hepatitis C virus (HCV) in a 48-week total treatment duration regimen following liver transplantation.

Interventions

  • DRUG Ribavirin
  • DRUG Telaprevir
  • DRUG Pegylated Interferon Alfa-2a
  • DRUG Immunosuppressant Regimen

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2012-02
Est. Completion 2014-04
Phase Phase 2

Sponsor

Vertex Pharmaceuticals Incorporated

191 total trials

What the Registry Record Tells You About NCT01467505

The ClinicalTrials.gov registry entry for NCT01467505 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 61 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 4 interventions - of which Ribavirin is the first listed.

NCT01467505 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01467505 about?

NCT01467505 is a clinical study titled "An Open Label Study of the Effect of Telaprevir in Combination With Ribavirin and Peginterferon on HCV Infection in Stable Liver Transplant Patients". To assess efficacy of telaprevir, pegylated interferon alfa-2a (Peg-IFN-alfa-2a), and ribavirin (RBV) for hepatitis C virus (HCV) in a 48-week total treatment duration regimen following liver transplantation.

What is the current status of trial NCT01467505?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 61 participants. The study started on 2012-02. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01467505?

The interventions under investigation include: Ribavirin (DRUG), Telaprevir (DRUG), Pegylated Interferon Alfa-2a (DRUG), Immunosuppressant Regimen (DRUG).

Who is sponsoring clinical trial NCT01467505?

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.