CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 214 enrolled
Drug / intervention
Bimekizumabdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04109976
NCT04109976Phase 3Completed

A Multicenter, Randomized, Open-Label Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or Auto-Injector for the Subcutaneous Self-Injection of Bimekizumab Solution by Subjects With Active Psoriatic Arthritis

UCB Biopharma SRL·interventional·Posted Oct 1, 2019·Updated Nov 30, 2023

In Brief

A Phase 3 clinical trial evaluating Bimekizumab for Psoriatic Arthritis. Completed, enrolled 214 participants across 47 sites in 6 countries.

Detailed Summary

The purpose of the study is to evaluate for each self-injecting device presentation the ability of subjects with psoriatic arthritis (PsA) to safely and effectively self-inject bimekizumab at study start and 4 weeks after training in self-injection technique using the bimekizumab safety syringe (SS) or the bimekizumab auto-injector (AI).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia, Germany, Hungary, Poland, Russia, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2020202120222023202420252026
First PostedOct 1, 2019
Enrollment StartAug 13, 2019
Primary CompletionNov 5, 2020
Study CompletionNov 13, 2020
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 6.8 years ago

Interventions

Bimekizumabdrug

Study participants will receive bimekizumab at pre-specified time points.