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COMPLETED Phase 3

An Efficacy and Safety Study of Two Dose Levels of Certolizumab Pegol (CZP) in Subjects With Plaque Psoriasis (PSO)

NCT02326298 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to investigate the efficacy and safety of two dose levels of certolizumab pegol in adults with moderate to severe chronic plaque psoriasis when administered every 2 weeks.

Interventions

  • OTHER Placebo
  • BIOLOGICAL Certolizumab Pegol

Study Locations (20)

Other

  • Ps0005 553 — Náchod
  • Ps0005 550 — Olomouc
  • Ps0005 551 — Ostrava-Poruba
  • Ps0005 552 — Prague

Ontario

  • Ps0005 596 — Ajax
  • Ps0005 590 — Hamilton
  • Ps0005 593 — Toronto

Quebec

  • Ps0005 595 — Drummondville
  • Ps0005 594 — Québec

California

  • Ps0005 504 — San Diego

Iowa

  • Ps0005 502 — West Des Moines

Louisiana

  • Ps0005 500 — Baton Rouge

Massachusetts

  • Ps0005 506 — Boston

Missouri

  • Ps0005 505 — St Louis

Trial Details

FieldValue
Enrollment Target 234 participants
Start Date 2014-12-16
Est. Completion 2018-10-24
Phase Phase 3

Sponsor

UCB Biopharma S.P.R.L.

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02326298

The ClinicalTrials.gov registry entry for NCT02326298 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 234 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Biopharma S.P.R.L., which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Psoriasis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02326298 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Ontario, Quebec. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02326298 about?

NCT02326298 is a clinical study titled "An Efficacy and Safety Study of Two Dose Levels of Certolizumab Pegol (CZP) in Subjects With Plaque Psoriasis (PSO)". The purpose of this study is to investigate the efficacy and safety of two dose levels of certolizumab pegol in adults with moderate to severe chronic plaque psoriasis when administered every 2 weeks.

What is the current status of trial NCT02326298?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 234 participants. The study started on 2014-12-16. Estimated completion is 2018-10-24.

What conditions does trial NCT02326298 study?

This clinical trial studies the following conditions: Psoriasis, Plaque Psoriasis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02326298?

The interventions under investigation include: Placebo (OTHER), Certolizumab Pegol (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02326298?

This trial is sponsored by UCB Biopharma S.P.R.L., which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02326298 being conducted?

This trial has 20 study locations across California, Iowa, Louisiana, Massachusetts, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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