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ACTIVE NOT RECRUITING Phase 3

A Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Subjects With Active Axial Spondyloarthritis Including Ankylosing Spondylitis and Nonradiographic Axial Spondyloarthritis

NCT04436640 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to demonstrate the long-term safety, tolerability and efficacy of bimekizumab in patients with active axial spondyloarthritis (axSpA, also known as radiographic axSpa (r-axSpA)) including ankylosing spondylitis (AS) and nonradiographic axial spondyloarthritis (nr-axSpa).

Interventions

  • DRUG Bimekizumab

Study Locations (20)

Other

  • As0014 40004 — Brussels
  • As0014 40003 — Genk
  • As0014 40001 — Ghent
  • As0014 40006 — Plovdiv
  • As0014 40007 — Plovdiv
  • As0014 40005 — Sofia
  • As0014 40008 — Sofia
  • As0014 20040 — Beijing
  • As0014 20021 — Chengdu
  • As0014 20019 — Guangzhou

Arizona

  • As0014 50062 — Glendale
  • As0014 50052 — Phoenix

Florida

  • As0014 50059 — Ormond Beach
  • As0014 50056 — Sarasota

California

  • As0014 50060 — Upland

Maryland

  • As0014 50015 — Hagerstown

Missouri

  • As0014 50016 — St Louis

Oregon

  • As0014 50055 — Portland

Pennsylvania

  • As0014 50020 — Duncansville

Trial Details

FieldValue
Enrollment Target 508 participants
Start Date 2020-06-16
Est. Completion 2026-08-07
Phase Phase 3

Sponsor

UCB Biopharma SRL

116 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04436640

The ClinicalTrials.gov registry entry for NCT04436640 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 508 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Biopharma SRL, which has 116 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Ankylosing Spondylitis appearing as the primary indexed condition, and to 1 intervention — of which Bimekizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04436640 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, Arizona, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04436640 about?

NCT04436640 is a clinical study titled "A Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Subjects With Active Axial Spondyloarthritis Including Ankylosing Spondylitis and Nonradiographic Axial Spondyloarthritis". The purpose of the study is to demonstrate the long-term safety, tolerability and efficacy of bimekizumab in patients with active axial spondyloarthritis (axSpA, also known as radiographic axSpa (r-axSpA)) including ankylosing spondylitis (AS) and nonradiographic axial spondyloarthritis (nr-axSpa).

What is the current status of trial NCT04436640?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 508 participants. The study started on 2020-06-16. Estimated completion is 2026-08-07.

What conditions does trial NCT04436640 study?

This clinical trial studies the following conditions: Ankylosing Spondylitis, Axial Spondyloarthritis, r-axSpa, Nr-axSpa. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04436640?

The interventions under investigation include: Bimekizumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04436640?

This trial is sponsored by UCB Biopharma SRL, which has 116 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04436640 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Maryland, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial