ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study With a Initial Treatment Period Followed by a Randomized-withdrawal Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT03410992

Public ClinicalTrials.gov record NCT03410992. 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 19, 2026, 11:10 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, Double-Blind, Placebo-Controlled Study With an Initial Treatment Period Followed by a Randomized-Withdrawal Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

Study identification

NCT ID
NCT03410992
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
435 participants

Conditions and interventions

Interventions

  • Bimekizumab Drug
  • Placebo Other

Drug · 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 4, 2018
Primary completion
Dec 27, 2018
Completion
Jan 6, 2020
Last update posted
Apr 14, 2026

2018 – 2020

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Ps0013 919 San Diego California 92103
Ps0013 955 San Diego California 92123
Ps0013 967 Santa Monica California 90404
Ps0013 928 Fort Myers Florida 33912
Ps0013 966 Sandy Springs Georgia 30329
Ps0013 954 Skokie Illinois 60077
Ps0013 962 Owensboro Kentucky 42303
Ps0013 944 New Orleans Louisiana 70115
Ps0013 940 Beverly Massachusetts 01915
Ps0013 901 Portsmouth New Hampshire 03801
Ps0013 956 Verona New Jersey 07044-2946
Ps0013 947 Buffalo New York 14221
Ps0013 968 New York New York 10021
Ps0013 965 New York New York 10025
Ps0013 963 Rochester New York 14623
Ps0013 949 Cleveland Ohio 44106-1716
Ps0013 929 Portland Oregon 97223
Ps0013 937 Johnston Rhode Island 02919
Ps0013 914 San Antonio Texas 78213
Ps0013 933 Murray Utah 84107

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 57 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03410992, 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 Apr 14, 2026 · Synced May 19, 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 NCT03410992 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →