drugset / Trial / NCT04452006

A Study in Healthy Subjects to Investigate the Safety and Tolerability of ACT- 541478 as Well as What ACT-541478 Does to the Body and the Way the Body Takes up, Distributes, and Gets Rid of ACT-541478

NCT04452006 ↗

Phase 1 Terminated 56 enrolled Idorsia Pharmaceuticals Ltd.
RandomizedParallel-groupQuadruple-blindOther

Summary

A study in healthy subjects to investigate the safety and tolerability of ACT-541478 as well as what ACT-541478 does to the body and the way the body takes up, distributes, and gets rid of of ACT-541478

Timeline

Start
2020-07-20
Primary completion
2021-04-20
Completion
2021-04-20

Outcome

Outcome not reported

Stopped: “Based on interim analysis, the Sponsor decided to terminate the study prematurely.”

Drugs

EvaluationDrugModalityDoseRoute
Subject ACT-541478 Unknown 10 mg Oral
Subject ACT-541478 Unknown 30 mg Oral
Subject ACT-541478 Unknown 100 mg Oral
Subject ACT-541478 Unknown 300 mg Oral
Subject ACT-541478 Unknown 1000 mg Oral

Indications

No indication recorded.