ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety Study of Certolizumab Pegol (CZP) Versus Active Comparator and Placebo in Subjects With Plaque Psoriasis (PSO)

ClinicalTrials.gov ID: NCT02346240

Public ClinicalTrials.gov record NCT02346240. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 3:33 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo- and Active-Controlled Study Followed by a Placebo-Controlled Maintenance Period and Open-Label Follow-Up to Evaluate the Efficacy and Safety of Certolizumab Pegol in Subjects With Moderate to Severe Chronic Plaque Psoriasis

Study identification

NCT ID
NCT02346240
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma S.P.R.L.
Industry
Enrollment
559 participants

Conditions and interventions

Interventions

  • Certolizumab Pegol Biological
  • Etanercept Biological
  • Placebo Other

Biological · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 10, 2015
Primary completion
Mar 21, 2016
Completion
Dec 16, 2018
Last update posted
Jul 15, 2021

2015 – 2018

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Ps0003 317 Mobile Alabama 36608
Ps0003 306 Little Rock Arkansas 72204
Ps0003 301 Beverly Hills California 90212
Ps0003 307 Los Angeles California 90045
Ps0003 405 San Diego California 92123
Ps0003 316 Washington D.C. District of Columbia 20037
Ps0003 304 West Palm Beach Florida 33409
Ps0003 302 Springfield Illinois 62703
Ps0003 313 West Dundee Illinois 60118
Ps0003 310 Indianapolis Indiana 46256
Ps0003 400 Henderson Nevada 89052
Ps0003 319 Verona New Jersey 07044-29
Ps0003 404 Buffalo New York 14203
Ps0003 407 Portland Oregon 97223
Ps0003 309 Johnston Rhode Island 02919
Ps0003 401 Dallas Texas 75246
Ps0003 403 Houston Texas 77065
Ps0003 406 San Antonio Texas 78213
Ps0003 311 Webster Texas 77598

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02346240, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 15, 2021 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02346240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →