drugset / Trial / NCT02222974

Single Increasing Dose Tolerance Study in Healthy Male Volunteers of BIIR 561 CL

NCT02222974 ↗

Phase 1 Completed 84 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

The objective of the study is to obtain information about safety, tolerability and pharmacokinetics of BIIR 561 CL after single intravenous administration of increasing doses in healthy male volunteers

Timeline

Start
1999-01
Primary completion
1999-08
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject IRAMPANEL Small molecule 1 mg Intravenous
Subject IRAMPANEL Small molecule 175 mg Intravenous

Indications

No indication recorded.