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ACTIVE NOT RECRUITING Phase 3

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Study Participants With Active Psoriatic Arthritis

NCT06624228 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to compare the efficacy of bimekizumab versus risankizumab after 16 weeks of treatment in study participants with active psoriatic arthritis (PsA).

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Bimekizumab
  • DRUG Risankizumab

Study Locations (20)

Florida

  • Pa0016 50630 — Clearwater
  • Pa0016 50679 — Cutler Bay
  • Pa0016 50685 — Fort Lauderdale
  • Pa0016 50059 — Ormond Beach
  • Pa0016 50324 — Plantation
  • Pa0016 50678 — Zephyrhills

Arizona

  • Pa0016 50662 — Gilbert
  • Pa0016 50062 — Glendale
  • Pa0016 50058 — Phoenix
  • Pa0016 50131 — Sun City

California

  • Pa0016 50654 — Covina
  • Pa0016 50663 — San Diego
  • Pa0016 50672 — Santa Monica

Illinois

  • Pa0016 50651 — Skokie
  • Pa0016 50650 — Willowbrook

Michigan

  • Pa0016 50665 — Lansing
  • Pa0016 50551 — Saint Clair Shores

Maryland

  • Pa0016 50686 — Hagerstown

Minnesota

  • Pa0016 50689 — Eagan

Missouri

  • Pa0016 50682 — Kansas City

Trial Details

FieldValue
Enrollment Target 684 participants
Start Date 2024-10-21
Est. Completion 2026-05-26
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 NCT06624228

The ClinicalTrials.gov registry entry for NCT06624228 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 684 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 1 condition, with Psoriatic Arthritis appearing as the primary indexed condition, and to 3 interventions — of which Placebo 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: NCT06624228 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, Arizona, California. 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 NCT06624228 about?

NCT06624228 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Study Participants With Active Psoriatic Arthritis". The purpose of the study is to compare the efficacy of bimekizumab versus risankizumab after 16 weeks of treatment in study participants with active psoriatic arthritis (PsA).

What is the current status of trial NCT06624228?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 684 participants. The study started on 2024-10-21. Estimated completion is 2026-05-26.

What conditions does trial NCT06624228 study?

This clinical trial studies the following conditions: Psoriatic Arthritis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06624228?

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

Who is sponsoring clinical trial NCT06624228?

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 NCT06624228 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Illinois, Maryland. 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