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Completed Phase 3 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Nonradiographic Axial Spondyloarthritis

ClinicalTrials.gov ID: NCT03928704

Public ClinicalTrials.gov record NCT03928704. 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 Oct 25, 2026, 5:42 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, Placebo-Controlled Study Evaluating the Efficacy and Safety of Bimekizumab in Subjects With Active Nonradiographic Axial Spondyloarthritis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to demonstrate the efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared to placebo in the treatment of subjects with active nonradiographic axial spondyloarthritis (nr-axSpA).

Study identification

NCT ID
NCT03928704
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
274 participants

Conditions and interventions

Interventions

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
Apr 25, 2019 (Actual)
Primary completion
Jun 29, 2022 (Actual)
Completion
Apr 17, 2023 (Actual)
Last update posted
Sep 25, 2026

2019 – 2023

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
As0010 50131 Mesa Arizona 85210 —
As0010 50052 Phoenix Arizona 85032 —
As0010 50062 Sun City Arizona 85351 —
As0010 50060 Upland California 91786 —
As0010 50059 Ormond Beach Florida 32174 —
As0010 50056 Sarasota Florida 34239 —
As0010 50015 Hagerstown Maryland 21740 —
As0010 50016 St Louis Missouri 63141 —
As0010 50055 Portland Oregon 97239-3011 —
As0010 50020 Duncansville Pennsylvania 16635 —
As0010 50012 Memphis Tennessee 38119-5214 —
As0010 50057 Dallas Texas 75231 —
As0010 50036 Mesquite Texas 75150 —
As0010 50061 Spokane Washington 99204 —

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 69 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03928704, 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 Sep 25, 2026 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03928704 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →