drugset / Trial / NCT02254083

Tolerability and Pharmacokinetics/-Dynamics of BIBT 986 BS in Healthy Male Subjects

NCT02254083 ↗

Phase 1 Completed 16 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Study to assess the tolerability of an intravenous infusion of 0.5 and 1.0 mg (actual 0.8 mg) BIBT 986 BS per hour over 32 hours as well as pharmacokinetics and the effect on blood coagulation parameters

Timeline

Start
2003-02
Primary completion
2003-05
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BIBT 986 BS Unknown 0.5 mg Intravenous
Subject BIBT 986 BS Unknown 0.8 mg Intravenous

Indications

No indication recorded.