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RECRUITING
NCT07801495
PHASE2

A Study to Assess the Efficacy, Safety and Tolerability of DDY391 in Participants With Moderate to Severe Psoriatic Arthritis

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

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

Interventions

DRUG

DDY391

DDY391

DRUG

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