ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT04242446

Public ClinicalTrials.gov record NCT04242446. 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 20, 2026, 2:38 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, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

Study identification

NCT ID
NCT04242446
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
505 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 18, 2020
Primary completion
Apr 6, 2022
Completion
Feb 18, 2023
Last update posted
May 18, 2026

2020 – 2023

United States locations

U.S. sites
28
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
Hs0003 50140 Birmingham Alabama 35233
Hs0003 50175 Phoenix Arizona 85006
Hs0003 50161 Los Angeles California 90045
Hs0003 50220 San Diego California 92123
Hs0003 50205 North Miami Beach Florida 33162-4708
Hs0003 50153 Ormond Beach Florida 32174
Hs0003 50141 Tampa Florida 33613
Hs0003 50210 Atlanta Georgia 30309
Hs0003 50280 Watkinsville Georgia 30677
Hs0003 50425 Murray Kentucky 42071
Hs0003 50198 Beverly Massachusetts 01915
Hs0003 50146 Boston Massachusetts 02215
Hs0003 50194 Omaha Nebraska 68144
Hs0003 50208 Las Vegas Nevada 89148
Hs0003 50137 East Windsor New Jersey 08520
Hs0003 50235 New York New York 10003
Hs0003 50151 Chapel Hill North Carolina 27516
Hs0003 50177 Cincinnati Ohio 45219
Hs0003 50138 Columbus Ohio 43213
Hs0003 50204 Tulsa Oklahoma 74135
Hs0003 50147 Hershey Pennsylvania 17033
Hs0003 50008 Johnston Rhode Island 02919
Hs0003 50180 Providence Rhode Island 02903
Hs0003 50142 Nashville Tennessee 37215
Hs0003 50201 Arlington Texas 76011
Hs0003 50166 Dallas Texas 75246
Hs0003 50149 San Antonio Texas 78213
Hs0003 50270 Seattle Washington 98101

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 60 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04242446, 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 May 18, 2026 · Synced May 20, 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 NCT04242446 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →