drugset / Trial / NCT02258971

Metabolism and Pharmacokinetics of [14C] BEA 2180 BR Administered Orally Compared to [14C] BEA 2180 BR Administered Intravenously in Healthy Male Volunteers

NCT02258971

Phase 1 Completed 14 enrolled Boehringer Ingelheim
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Primary objectives: To determine the basic pharmacokinetics of BEA 2180 BR, its metabolites CD 1975 ZW and CD 1976 ZW and radioactivity including excretion mass balance, excretion pathways and metabolism following the oral and intravenous administration of \[14C\] BEA 2180 BR Secondary objectives: To determine safety and tolerability following single dose oral and iv administration of BEA 2180 BR in healthy male volunteers.

Timeline

Start
2007-03
Primary completion
2007-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BEA 2180 BR Unknown 500 ug Oral
Subject BEA 2180 BR Unknown 1200 ug Oral

Indications

No indication recorded.