drugset / Trial / NCT02254135

Study to Assess Safety, Tolerability and Pharmacokinetics of Single Rising Doses of BEA 2180 BR in Healthy Male Volunteers

NCT02254135

Phase 1 Completed 24 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

Study to investigate safety, tolerability, and pharmacokinetics of single rising peroral doses of BEA 2180 BR

Timeline

Start
2006-12
Primary completion
2007-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BEA 2180 BR Unknown 400 ug Oral
Subject BEA 2180 BR Unknown 800 ug Oral
Subject BEA 2180 BR Unknown 1200 ug Oral

Indications

No indication recorded.