drugset / Trial / NCT02244203

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BI 60732 in Healthy Male Volunteers

NCT02244203 ↗

Phase 1 Completed 56 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindTreatment

Summary

Single Rising Dose (SRD) study: First evaluation of safety, tolerability, pharmacokinetics and pharmacodynamics of BI 60732

Timeline

Start
2009-02
Primary completion
2009-07
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 60732 Unknown 0.25 mg —
Subject BI 60732 Unknown 0.5 mg —
Subject BI 60732 Unknown 1 mg —
Subject BI 60732 Unknown 2 mg —
Subject BI 60732 Unknown 4 mg —
Subject BI 60732 Unknown 20 mg —
Subject BI 60732 Unknown 50 mg —
Subject BI 60732 Unknown 100 mg —
Subject BI 60732 Unknown 150 mg —
Subject BI 60732 Unknown 200 mg —

Indications

No indication recorded.