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NCT00160641 · ClinicalTrials.gov registry record · Phase 3

A Study of the Safety and Effectiveness of Liquid Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis

A Phase 3 study, sponsored by UCB Pharma.

Completed
Registry status
Phase 3
Development phase
567
Enrollment target

NCT00160641: Completed Phase 3 study, sponsored by UCB Pharma.

NCT00160641 is a Phase 3 study that has completed, run by UCB Pharma. The registered enrollment target is 567 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00160641, a Phase 3 study, has completed, sponsored by UCB Pharma.

COMPLETED
Registry status
Phase 3
Development phase
567 participants
Enrollment target

Study Summary

An open ended study in which patients who completed the preceding double-blind study NCT00160602 are given Certolizumab Pegol and assessed for signs and symptoms of Rheumatoid Arthritis.

Primary Outcome

An AE is any untoward medical occurrence in a subject or trial subject that is administered a drug or biologic (medicinal product) or that is using a medical device. The event does not necessarily have a causal relationship with that treatment or usage. First dose of CZP was at Baseline of the preceding double-blind study NCT00160602 for subjects randomized to CZP, or at Entry Visit (Week 0) of this study for subjects randomized to Placebo.

Interventions

  • BIOLOGICAL Certolizumab Pegol

Trial Details

FieldValue
Enrollment Target 567 participants
Start Date 2005-11
Est. Completion 2012-02
Phase Phase 3
UCB Pharma

100 total trials

What the finished NCT00160641 record still lists

NCT00160641 is an interventional study that assigns participants to a tested intervention. The registered 567 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 (27% lower).

The record links to 0 conditions, and to 1 intervention - of which Certolizumab Pegol is the first listed.

NCT00160641 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00160641 about?

NCT00160641 is a clinical study titled "A Study of the Safety and Effectiveness of Liquid Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis". An open ended study in which patients who completed the preceding double-blind study NCT00160602 are given Certolizumab Pegol and assessed for signs and symptoms of Rheumatoid Arthritis.

What is the current status of trial NCT00160641?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 567 participants. The study started on 2005-11. Estimated completion is 2012-02.

What interventions are being tested in trial NCT00160641?

The interventions under investigation include: Certolizumab Pegol (BIOLOGICAL).

Who is sponsoring clinical trial NCT00160641?

This trial is sponsored by UCB Pharma, which has 100 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00160641's enrollment target sits among peer trials

567 667th of 2000 higher than 1,334 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 NCT00160641, the US trial registry maintained by the National Library of Medicine. NCT00160641 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.