drugset / Trial / NCT02171533

Relative Bioavailability of Single Oral Doses of Dabigatran Etexilate With or Without Oral Administration of Verapamil in Two Different Dosages in Healthy Male and Female Volunteers

NCT02171533

Phase 1 Completed 40 enrolled Boehringer Ingelheim
RandomizedCrossoverOpen-labelTreatment

Summary

To investigate whether and to what extent the P-glycoprotein inhibitor (P-gp) verapamil affects the pharmacokinetic parameters of dabigatran with verapamil given at different dosages, in different formulations (immediate release (IR) and extended release (ER)), and in different intervals in relation to the dabigatran dose.

Timeline

Start
2008-06
Primary completion
2008-08
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabigatran Unknown 150 mg Oral
Subject Verapamil Other / unclassified 120 mg Oral
Subject Verapamil Other / unclassified 240 mg Oral
Subject Verapamil Other / unclassified 480 mg Oral

Indications

No indication recorded.