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A Study to Assess the Efficacy, Safety and Tolerability of DDY391 in Participants With Moderate to Severe Psoriatic Arthritis
Sponsor: Novartis Pharmaceuticals
Summary
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.
Official title: A Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2a/b Study Assessing the Efficacy, Safety and Tolerability of DDY391 in Participants With Active Moderate to Severe Psoriatic Arthritis
Key Details
Gender
All
Age Range
18 Years - 100 Years
Study Type
INTERVENTIONAL
Enrollment
220
Start Date
2026-10-14
Completion Date
2029-01-12
Last Updated
2026-10-13
Healthy Volunteers
No
Conditions
Interventions
DDY391
DDY391
Placebo
Matching placebo
Locations (3)
Shelby Research LLC
Memphis, Tennessee, United States
Precision Comprehensive Research
Colleyville, Texas, United States
Rheumatology Associates of South Texas
San Antonio, Texas, United States