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NCT03895203 · ClinicalTrials.gov registry record · Phase 3

A Study to Test the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis

A Phase 3 study, sponsored by UCB Biopharma SRL.

Completed
Registry status
Phase 3
Development phase
852
Enrollment target

NCT03895203: Completed Phase 3 study, sponsored by UCB Biopharma SRL.

NCT03895203 is a Phase 3 study that has completed, run by UCB Biopharma SRL. The registered enrollment target is 852 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (10% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03895203, a Phase 3 study, has completed, sponsored by UCB Biopharma SRL.

COMPLETED
Registry status
Phase 3
Development phase
852 participants
Enrollment target

Study Summary

This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of subjects with active Psoriatic Arthritis (PsA).

Primary Outcome

ACR50 response rate: 50% or greater improvement of arthritis relative to Baseline. Those who met following 3 conditions for improvement from Baseline were classified as meeting ACR50 response criteria: greater than or equal (≥) 50% improvement in 68-tender joint count; ≥ 50% improvement in 66-swollen joint count; ≥ 50% improvement in at least 3 of 5 following parameters: Physician global assessment of disease activity (0-100 millimeter \[mm\] visual analog scale \[VAS\] \[0 = no symptoms;100 = s

Interventions

  • OTHER Placebo
  • DRUG Adalimumab
  • DRUG Bimekizumab

Trial Details

FieldValue
Enrollment Target 852 participants
Start Date 2019-04-03
Est. Completion 2022-07-11
Phase Phase 3
UCB Biopharma SRL

82 total trials

What the finished NCT03895203 record still lists

NCT03895203 is an interventional study that assigns participants to a tested intervention. The registered 852 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (10% higher).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT03895203 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03895203 about?

NCT03895203 is a clinical study titled "A Study to Test the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis". This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of subjects with active Psoriatic Arthritis (PsA).

What is the current status of trial NCT03895203?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 852 participants. The study started on 2019-04-03. Estimated completion is 2022-07-11.

What interventions are being tested in trial NCT03895203?

The interventions under investigation include: Placebo (OTHER), Adalimumab (DRUG), Bimekizumab (DRUG).

Who is sponsoring clinical trial NCT03895203?

This trial is sponsored by UCB Biopharma SRL, which has 82 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03895203's enrollment target sits among peer trials

852 385th of 2000 higher than 1,615 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03895203, the US trial registry maintained by the National Library of Medicine. NCT03895203 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.