drugset / Trial / NCT01241539

Pharmacokinetics of Dabigatran Etexilate (Pradaxa®) During Haemodialysis

NCT01241539

Phase 1 Completed 7 enrolled Boehringer Ingelheim
Non-randomizedSingle-groupOpen-label

Summary

The current study will allow the assessment of pharmacokinetics, pharmacodynamics, elimination rate and clearance of dabigatran etexilate during and following haemodialysis in ESRD patients.

Timeline

Start
2010-11
Primary completion
2011-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Dabigatran etexilate Unknown 75 mg Oral
Subject Dabigatran etexilate Unknown 110 mg Oral
Subject Dabigatran etexilate Unknown 150 mg Oral