drugset / Trial / NCT02223507

Single Dose Followed by Maintenance Dose Tolerance Study of BIIR 561 CL in Healthy Elderly Male and Female Volunteers

NCT02223507 ↗

Phase 1 Completed 13 enrolled Boehringer Ingelheim
RandomizedParallel-groupSingle-blindTreatment

Summary

The objective of the present study was to obtain information about the safety, tolerability and pharmacokinetics of BIIR 561 CL after continuous intravenous administration of two increasing doses in healthy elderly volunteers, following the infusion schema of a loading dose (1 hour) and a maintenance dose (5 hours)

Timeline

Start
2000-08
Primary completion
2000-09
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject IRAMPANEL Small molecule 40 mg Intravenous
Subject IRAMPANEL Small molecule 75 mg Intravenous

Indications

No indication recorded.