drugset / Trial / NCT02170792

Bioavailability of BIBR 953 ZW After Dose of BIBR 1048 MS

NCT02170792

Phase 1 Completed 30 enrolled Boehringer Ingelheim
RandomizedCrossoverOpen-labelTreatment

Summary

To assess the extent of absorption of 12.5, 50 and 200 mg of BIBR 1048 MS with and without coadministration of 150 mg ranitidine.

Timeline

Start
2001-02
Primary completion
2001-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabigatran etexilate Unknown 12.5 mg Oral
Subject Dabigatran etexilate Unknown 50 mg Oral
Subject Dabigatran etexilate Unknown 200 mg Oral
Subject Ranitidine Unknown 150 mg

Indications

No indication recorded.