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Completed Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT03412747

Public ClinicalTrials.gov record NCT03412747. 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, Randomized, Double-Blind Study With an Active-Controlled Initial Treatment Period Followed by a Dose-Blind Maintenance Treatment Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

Study identification

NCT ID
NCT03412747
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
478 participants

Conditions and interventions

Interventions

  • Adalimumab Drug
  • 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
Jan 25, 2018
Primary completion
Feb 6, 2019
Completion
Feb 25, 2020
Last update posted
Apr 14, 2026

2018 – 2020

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Ps0008 957 Glendale Arizona 85308
Ps0008 927 Los Angeles California 90033
Ps0008 955 San Diego California 92123
Ps0008 943 San Luis Obispo California 93405
Ps0008 967 Santa Monica California 90404
Ps0008 939 Danbury Connecticut 06810
Ps0008 934 Washington D.C. District of Columbia 20037
Ps0008 906 Boca Raton Florida 33486
Ps0008 936 Tampa Florida 33624
Ps0008 900 West Des Moines Iowa 50265
Ps0008 905 Overland Park Kansas 66215
Ps0008 940 Beverly Massachusetts 01844
Ps0008 925 Brighton Massachusetts 02135
Ps0008 917 Troy Michigan 48084
Ps0008 908 East Windsor New Jersey 08520
Ps0008 961 Rocky Mount North Carolina 27804
Ps0008 935 Winston-Salem North Carolina 27104-35 20
Ps0008 932 Oklahoma City Oklahoma 73112
Ps0008 929 Portland Oregon 97223
Ps0008 945 Greer South Carolina 29650
Ps0008 931 Dallas Texas 75231
Ps0008 924 Houston Texas 77004
Ps0008 951 Houston Texas 77004

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 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03412747, 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 NCT03412747 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →