drugset / Trial / NCT06550076

A Study of TAK-279 in Participants With Moderate-to-Severe Plaque Psoriasis

NCT06550076

Phase 3 Active not recruiting 2099 enrolled Takeda
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The main aim of this study is to check the side effects of TAK-279 and how well it is tolerated in participants with moderate-to-severe plaque psoriasis. All participants will be assigned to study treatments of TAK-279 and will be treated with TAK-279 if the participants meet the study rules. Participants will be in the study for up to 217 weeks, including up to 35 days for the screening period, 52 weeks (Part A) up to 156 additional weeks (Part B) study treatment and 4 weeks follow up period. During the study, participants will visit their study clinic multiple times.

Timeline

Start
2024-09-04
Primary completion
2029-08-05
Completion
2029-08-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Zasocitinib Small molecule Oral

Indications