drugset / Trial / NCT02222961

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

NCT02222961 ↗

Phase 1 Completed 60 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

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

Timeline

Start
1999-11
Primary completion
2000-06
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject IRAMPANEL Small molecule 20 mg Intravenous
Subject IRAMPANEL Small molecule 40 mg Intravenous
Subject IRAMPANEL Small molecule 125 mg Intravenous

Indications

No indication recorded.