drugset / Trial / NCT02173717

Relative Bioavailability of Single Doses of Dabigatran Etexilate in Healthy Volunteers

NCT02173717

Phase 1 Completed 24 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

Study to investigate whether and to what extent the suggested P-glycoprotein (P-gp) inducer rifampicin affects plasma exposure of dabigatran.

Timeline

Start
2009-06
Primary completion
2009-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabigatran etexilate Unknown 150 mg Oral
Subject Rifampin Small molecule 600 mg Oral

Indications

No indication recorded.