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Completed Phase 2 Interventional Results available

A Study to Evaluate the Dose Response Based on the Efficacy, Safety and Tolerability of Bimekizumab in Subjects With Active Psoriatic Arthritis Which is a Type of Inflammatory Arthritis

ClinicalTrials.gov ID: NCT02969525

Public ClinicalTrials.gov record NCT02969525. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 1:41 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Phase 2B, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study to Evaluate the Efficacy and Safety of Bimekizumab in Active Psoriatic Arthritis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a study to evaluate the dose response based on the efficacy, safety and tolerability of bimekizumab in subjects with active psoriatic arthritis.

Study identification

NCT ID
NCT02969525
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Biopharma S.P.R.L.
Industry
Enrollment
206 participants

Conditions and interventions

Interventions

Other · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2016 (Actual)
Primary completion
Nov 2017 (Actual)
Completion
Jul 2018 (Actual)
Last update posted
Mar 20, 2023

2016 – 2018

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Pa0008 007 San Diego California 92037 —
Pa0008 005 Aventura Florida 33180 —
Pa0008 003 Hagerstown Maryland 21740 —
Pa0008 011 Lansing Minnesota 48910 —
Pa0008 025 Lexington New York 40504 —
Pa0008 014 Portland Oregon 97239 —
Pa0008 001 Duncansville Pennsylvania 16635 —
Pa0008 012 Johnston Rhode Island 02919 —
Pa0008 004 Charleston South Carolina 29406-93 —
Pa0008 010 Jackson Tennessee 38305 —
Pa0008 006 Dallas Texas 75231 —
Pa0008 013 Mesquite Texas 75150 —
Pa0008 002 Seattle Washington 98122 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02969525, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 20, 2023 · Synced Oct 28, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02969525 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →