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NCT01853254 · ClinicalTrials.gov registry record · Phase 3

A Study of Pegasys (Peginterferon Alfa-2a) Administered Alone or in Combination With Copegus (Ribavirin) in Patients With Chronic Hepatitis C Who Have Participated in Previous Pegasys Trials

A Phase 3 study, sponsored by Hoffmann-La Roche.

Completed
Registry status
Phase 3
Development phase
272
Enrollment target

NCT01853254: Completed Phase 3 study, sponsored by Hoffmann-La Roche.

NCT01853254 is a Phase 3 study that has completed, run by Hoffmann-La Roche. The registered enrollment target is 272 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01853254, a Phase 3 study, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
Phase 3
Development phase
272 participants
Enrollment target

Study Summary

This open-label, non-randomized, single arm study will provide treatment or re-treatment with Pegasys (peginterferon alfa-2a) as monotherapy or in combination with Copegus (ribavirin) to patients with chronic hepatitis C infection. Patients who have received prior Pegasys monotherapy or combination therapy or who were considered eligible for treatment with Pegasys in previous donor protocols will be eligible to participate in this study. Treatment will be on investigator's decision according to the approved label for up to 48 weeks, with a 24-week safety follow-up.

Interventions

  • DRUG Ribavirin
  • DRUG Peginterferon alfa-2a

Trial Details

FieldValue
Enrollment Target 272 participants
Start Date 2003-09
Est. Completion 2011-09
Phase Phase 3
Hoffmann-La Roche

909 total trials

What the finished NCT01853254 record still lists

NCT01853254 is an interventional study that assigns participants to a tested intervention. The registered 272 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (65% lower).

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

NCT01853254 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01853254 about?

NCT01853254 is a clinical study titled "A Study of Pegasys (Peginterferon Alfa-2a) Administered Alone or in Combination With Copegus (Ribavirin) in Patients With Chronic Hepatitis C Who Have Participated in Previous Pegasys Trials". This open-label, non-randomized, single arm study will provide treatment or re-treatment with Pegasys (peginterferon alfa-2a) as monotherapy or in combination with Copegus (ribavirin) to patients with chronic hepatitis C infection. Patients who have received prior Pegasys monotherapy or combination ...

What is the current status of trial NCT01853254?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 272 participants. The study started on 2003-09. Estimated completion is 2011-09.

What interventions are being tested in trial NCT01853254?

The interventions under investigation include: Ribavirin (DRUG), Peginterferon alfa-2a (DRUG).

Who is sponsoring clinical trial NCT01853254?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01853254's enrollment target sits among peer trials

272 1214th of 2000 higher than 785 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT01853254, the US trial registry maintained by the National Library of Medicine. NCT01853254 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.