drugset / Trial / NCT03430661

A Study to Investigate the Interaction Between ACT-246475 and Clopidogrel, Prasugrel, and Ticagrelor in Healthy Subjects

NCT03430661

Phase 1 Completed 77 enrolled Viatris Innovation GmbH
RandomizedParallel-groupTriple-blindOther

Summary

The primary objective of this study is to assess the pharmacodynamic (PD) effects of clopidogrel, prasugrel, and ticagrelor when administered after a single subcutaneous (s.c.) dose of ACT-246475 in healthy male and female subjects

Timeline

Start
2018-01-24
Primary completion
2019-05-20
Completion
2019-05-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Clopidogrel Small molecule 300 mg Oral
Subject Clopidogrel Small molecule 600 mg Oral
Subject Prasugrel Small molecule 60 mg Oral
Subject Selatogrel Small molecule 16 mg Subcutaneous
Subject Ticagrelor Small molecule 180 mg Oral

Indications

No indication recorded.