drugset / Trial / NCT05715125

VTX958 Versus Placebo for the Treatment of Active Psoriatic Arthritis (Tranquility-PsA)

NCT05715125 ↗

Phase 2 Terminated 205 enrolled Ventyx Biosciences, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate if VTX958 is safe and effective in adult participants with active Psoriatic Arthritis. Approximately 195 eligible participants will take VTX958 Dose A, VTX958 Dose B, or matching placebo (no active drug) for 16 weeks and then move on to a 36 week Long Term Extension (LTE). The study will include 16 weeks of treatment, 36 weeks of LTE, and a 30-day follow-up period.

Timeline

Start
2023-01-31
Primary completion
2024-01-02
Completion
2024-01-02

Outcome

Outcome not reported

Stopped (Business): “sponsor decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject CENACITINIB Small molecule — —

Indications