Phase 3 Psoriasis Trial, Completed NCT03412747 Sponsor: UCB Biopharma SRL Condition: Psoriasis
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Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial enrolled 478 adults with psoriasis across three groups: one group received bimekizumab every four weeks and then switched to every four or eight weeks (161 people), a second group received bimekizumab every four weeks throughout (158 people), and a third group received adalimumab (159 people). The trial was measuring changes in psoriasis severity using two main scoring tools — a detailed skin assessment called the PASI score (which rates redness, thickness, and scaling across the body on a scale of 0 to 72), and a doctor's overall rating called the IGA (rated 0 to 4, from clear to severe). The trial ran for 56 weeks in total. The reported data shows that at week 16, when the two bimekizumab groups were combined for comparison against adalimumab, 86.2% of bimekizumab participants had at least a 90% improvement in their PASI score, compared with 47.2% in the adalimumab group. For the doctor's overall rating at week 16, 85.3% of bimekizumab participants were rated as "clear" or "almost clear" compared with 57.2% in the adalimumab group. At week 4, 76.5% of the bimekizumab group had at least a 75% improvement in their PASI score versus 31.4% for adalimumab, and by week 16, 60.8% of bimekizumab participants had a complete 100% improvement in their PASI score compared with 23.9% for adalimumab. The reported data also shows that at week 24, results were similar across both bimekizumab dosing schedules — roughly 85–86% of participants in each bimekizumab group had at least a 90% PASI improvement, and around 86–87% were rated "clear" by their doctor, compared with approximately 52% and 58% respectively in the adalimumab group. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 3 Psoriasis Trial, Completed

NCT03412747
Completed Phase 3 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be at least 18 years old
  • You have had chronic plaque psoriasis for at least 6 months before the screening visit
  • Your psoriasis is considered moderate to severe, based on specific medical measurements of how much of your body is affected and how severe it looks (confirm with trial site)
  • Your doctor has determined that you need a full-body (systemic) treatment or light therapy for your psoriasis
  • If you are a woman who could become pregnant, you must be willing to use a highly effective form of birth control during the trial

Who may not be able to join:

  • You have a known allergy or sensitivity to the ingredients in either of the study drugs (bimekizumab or adalimumab)
  • You currently have an infection (other than a common cold), have had a serious infection, or have a history of infections that keep coming back or are hard to treat
  • You currently have or have had hepatitis B, hepatitis C, or HIV
  • You have tuberculosis (TB), are at high risk of getting TB, or have had a related type of bacterial infection
  • You have another medical or mental health condition that the study doctor believes would make it unsafe or unsuitable for you to participate
  • You have previously been treated with the drug adalimumab
  • You are currently having thoughts of suicide or self-harm
  • You are currently experiencing moderate or severe major depression
  • You have had cancer in the last 5 years — except for certain treated and fully cured skin cancers or early-stage cervical cancer

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: UCB Cares, +1 844 599 2273 (UCB)

Australian sites

Ps0008 008, East Melbourne,
Ps0008 004, Fremantle,
Ps0008 007, Hectorville,
Ps0008 010, Kogarah,
Ps0008 005, Phillip,
Ps0008 009, Woolloongabba,

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Completed
Phase
Phase 3
Sponsor
UCB Biopharma SRL
Registry
ClinicalTrials.gov
Start date
26 January 2018
Est. completion
7 February 2019

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇩🇪 Germany 🇭🇺 Hungary 🇵🇱 Poland 🇷🇺 Russia 🇰🇷 South Korea 🇹🇼 Taiwan 🇺🇸 United States

6 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Percentage of Participants With a Psoriasis Area and Severity Index 90 (PASI90) Response at Week 16; Percentage of Participants With an Investigator's Global Assessment (IGA) Response (Clear or Almost Clear With at Least 2-Category Improvement Relative to Baseline) at Week 16

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov