drugset / Trial / NCT05976321

A Study of TAK-279 in Adults With or Without Liver Damage

NCT05976321

Phase 1 Completed 27 enrolled Takeda
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The main aim of this study is to find out how the body processes 1 dose of TAK-279 (pharmacokinetics) in participants with liver problems compared to participants without liver problems. Other aims are to check for side effects from TAK-279 and to learn how well participants tolerate 1 dose of TAK-279. The participants will need to stay at the clinic for 11 days.

Timeline

Start
2023-09-22
Primary completion
2024-04-15
Completion
2024-04-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Zasocitinib Small molecule 50 mg Oral

Indications

No indication recorded.