Status: Recruiting
A Study to Assess the Efficacy, Safety and Tolerability of DDY391 in Participants With Moderate to Severe Psoriatic Arthritis
The purpose of this Phase 2a/b study is: 1. to evaluate the efficacy, safety and tolerability of DDY391 in participants with psoriatic arthritis (PsA). 2. to determine the dose-response relationship of DDY391 in participants with PsA to support dose selection for Phase 3.
Participants needed: 220
Trial details
Phase: Phase 2Age: 18-100Biological sex: AllType: InterventionalSponsor: Novartis PharmaceuticalsUpdated: Oct 13, 2026Locations: 3
Eligibility criteria
Female or male participants at least 18 years of age. [+2]
Presence of inflammatory conditions other than psoriasis or PsA including but no... [+5]