drugset / Trial / NCT03410992

A Study With a Initial Treatment Period Followed by a Randomized-withdrawal Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasis

NCT03410992 ↗

Phase 3 Completed 435 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Phase 3 study to compare the efficacy of bimekizumab versus placebo in the treatment of subjects with moderate to severe chronic plaque psoriasis.

Timeline

Start
2018-02-05
Primary completion
2018-12-28
Completion
2020-01-07

Outcome

Met primary endpoint

paper Coprimary endpoints were met: PMID 33549192 ↗

paper 317 (91%) of 349 patients receiving bimekizumab 320 mg every 4 weeks achieved PASI90, compared with one (1%) of 86 patients receiving placebo PMID 33549192 ↗

paper 323 (93%) of 349 patients receiving bimekizumab 320 mg every 4 weeks achieved an IGA score of 0 or 1 versus one (1%) of 86 patients receiving placebo PMID 33549192 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 320 mg Other