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Safety and PK of Irampanel (BIIR 561) in Healthy Male Volunteers
NCT02222961Phase 1Completed
- Sponsor
- Boehringer Ingelheim
- Start
- Nov 1999
- Primary completion
- Jun 2000
- Modality
- Small Molecules
01
Overview
Phase 1, randomised, single-blind trial in acute ischemic stroke (AIS) comparing BIIR 561 CL with Placebo (2 arms). Primary endpoints: Number of subjects with adverse events up to 8 days, Number of subjects with clinically significant findings in vital functions up to 8 days and 2 more. Started Nov 1999; status: completed.
02
Drugs
irampanel
03
Conditions
acute ischemic stroke (AIS)
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