BENITIONSClinical Trial Intelligence

A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic Arthritis Including Those Who Have a History of Inadequate Response or Intolerance to Biologic Therapy(Ies)

Phase 3 Completed NCT03671148

ConditionPsoriatic Arthritis
PhasePhase 3
SponsorAbbVie
StatusCompleted
Enrollment444 participants
InterventionsRisankizumab
Start dateMar 7, 2019
Completion dateJun 22, 2020
Results postedMar 2, 2022

Summary

The purpose of this study is to evaluate the safety and efficacy of risankizumab in adults with moderately to severely active psoriatic arthritis (PsA).

Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 24

Baseline and Week 24 · percentage of participants

Placebo26.5 percentage of participants
Risankizumab51.3 percentage of participants
p-value<0.001
Response Rate Difference24.5 (95% CI 15.9–33.0)

Open in BENITIONS View on ClinicalTrials.gov

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