drugset / Trial / NCT01195688

Safety and Tolerability of BI 638683 After Single Rising Oral Doses in Healthy Male Subjects

NCT01195688 ↗

Phase 1 Completed 63 enrolled Boehringer Ingelheim
RandomizedSingle-groupDouble-blindTreatment

Summary

The primary objective of the current study is to investigate the safety and tolerability of BI 638683 in healthy male volunteers following oral administration of single rising doses

Timeline

Start
2010-09
Primary completion
2010-12
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 638683 Unknown — Oral

Indications

No indication recorded.