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NCT03370133 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Placebo and an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

A Phase 3 study, sponsored by UCB Biopharma SRL.

Completed
Registry status
Phase 3
Development phase
567
Enrollment target

NCT03370133: Completed Phase 3 study, sponsored by UCB Biopharma SRL.

NCT03370133 is a Phase 3 study that has completed, run by UCB Biopharma SRL. The registered enrollment target is 567 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03370133, a Phase 3 study, has completed, sponsored by UCB Biopharma SRL.

COMPLETED
Registry status
Phase 3
Development phase
567 participants
Enrollment target

Study Summary

This is a study to compare the efficacy of bimekizumab versus placebo and an active comparator in the treatment of subjects with moderate to severe chronic plaque psoriasis (PSO).

Primary Outcome

The PASI90 response assessments are based on at least 90% improvement in the PASI score from Baseline. This is a scoring system that averages the redness, thickness, and scaliness of the psoriatic lesions (on a 0-4 scale), and weights the resulting score by the area of skin involved. Body divided into 4 areas: head, arms, trunk to groin, and legs to top of buttocks. Assignment of an average score for the redness, thickness, and scaling for each of the 4 body areas with a score of 0 (clear) to 4

Interventions

  • DRUG Ustekinumab
  • OTHER Placebo
  • DRUG Bimekizumab

Trial Details

FieldValue
Enrollment Target 567 participants
Start Date 2017-12-06
Est. Completion 2019-12-13
Phase Phase 3
UCB Biopharma SRL

82 total trials

What the finished NCT03370133 record still lists

NCT03370133 is an interventional study that assigns participants to a tested intervention. The registered 567 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (27% lower).

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

NCT03370133 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03370133 about?

NCT03370133 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Placebo and an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis". This is a study to compare the efficacy of bimekizumab versus placebo and an active comparator in the treatment of subjects with moderate to severe chronic plaque psoriasis (PSO).

What is the current status of trial NCT03370133?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 567 participants. The study started on 2017-12-06. Estimated completion is 2019-12-13.

What interventions are being tested in trial NCT03370133?

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

Who is sponsoring clinical trial NCT03370133?

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 NCT03370133's enrollment target sits among peer trials

567 667th of 2000 higher than 1,334 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 NCT03370133, the US trial registry maintained by the National Library of Medicine. NCT03370133 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.