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NCT02552212 · ClinicalTrials.gov registry record · Phase 3

Multicenter Study Evaluating Certolizumab Pegol Compared to Placebo in Subjects With axSpA Without X-ray Evidence of AS

A Phase 3 study, sponsored by UCB Biosciences.

Completed
Registry status
Phase 3
Development phase
317
Enrollment target

NCT02552212 is a Phase 3 study that has completed, run by UCB Biosciences. The registered enrollment target is 317 participants.

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The verdict

NCT02552212, a Phase 3 study, has completed, sponsored by UCB Biosciences.

COMPLETED
Registry status
Phase 3
Development phase
317 participants
Enrollment target

Study Summary

Patients with active Axial Spondyloarthritis without x-ray evidence of Ankylosing Spondylitis and with signs of inflammation will be randomly assigned to receive certolizumab pegol (CZP) 200 mg every two weeks or placebo. The primary objective is to demonstrate the efficacy of CZP in these patients.

Interventions

  • OTHER Placebo
  • BIOLOGICAL Certolizumab Pegol

Trial Details

FieldValue
Enrollment Target 317 participants
Start Date 2015-09
Est. Completion 2020-05
Phase Phase 3

Sponsor

UCB Biosciences

39 total trials

What the Registry Record Tells You About NCT02552212

The ClinicalTrials.gov registry entry for NCT02552212 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 317 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Biosciences, which has 39 total studies on file at ClinicalTrials.gov.

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

NCT02552212 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02552212 about?

NCT02552212 is a clinical study titled "Multicenter Study Evaluating Certolizumab Pegol Compared to Placebo in Subjects With axSpA Without X-ray Evidence of AS". Patients with active Axial Spondyloarthritis without x-ray evidence of Ankylosing Spondylitis and with signs of inflammation will be randomly assigned to receive certolizumab pegol (CZP) 200 mg every two weeks or placebo. The primary objective is to demonstrate the efficacy of CZP in these patients.

What is the current status of trial NCT02552212?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 317 participants. The study started on 2015-09. Estimated completion is 2020-05.

What interventions are being tested in trial NCT02552212?

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

Who is sponsoring clinical trial NCT02552212?

This trial is sponsored by UCB Biosciences, which has 39 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.