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: NCT04242498

Public ClinicalTrials.gov record NCT04242498. 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
NCT04242498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
509 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
Mar 1, 2020
Primary completion
Nov 8, 2021
Completion
Sep 27, 2022
Last update posted
May 18, 2026

2020 – 2022

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Hs0004 50162 Fountain Valley California 92708
Hs0004 50196 Thousand Oaks California 91320
Hs0004 50199 Miami Florida 33125
Hs0004 50152 Orange Park Florida 32073
Hs0004 50144 Orlando Florida 38219
Hs0004 50184 Pembroke Pines Florida 33028
Hs0004 50193 Sandy Springs Georgia 30328
Hs0004 50223 Savannah Georgia 31419
Hs0004 50164 Skokie Illinois 60077
Hs0004 50234 Plainfield Indiana 46168
Hs0004 50178 Clarkston Michigan 48346
Hs0004 50105 St Louis Missouri 63110
Hs0004 50197 Henderson Nevada 89052
Hs0004 50159 Portsmouth New Hampshire 03801
Hs0004 50200 Verona New Jersey 07044
Hs0004 50237 Albuquerque New Mexico 87106
Hs0004 50211 Durham North Carolina 27710
Hs0004 50179 Winston-Salem North Carolina 27104
Hs0004 50145 Columbus Ohio 43230
Hs0004 50202 Fairborn Ohio 45324
Hs0004 50150 Philadelphia Pennsylvania 19103
Hs0004 50236 Greenville South Carolina 29615
Hs0004 50084 Johns Island South Carolina 29425
Hs0004 50148 Pflugerville Texas 78660

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 67 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04242498, 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

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04242498 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →