drugset / Trial / NCT02199899

Safety, Tolerability and Pharmacodynamics of BIIF 1149 BS in Healthy Young Male Volunteers

NCT02199899 ↗

Phase 1 Completed 64 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of the present study is to obtain information about the safety and tolerability of BIIF 1149 BS, to determine the pharmacologically active dose (range) by performing a citric acid challenge test and to obtain preliminary pharmacokinetic data

Timeline

Start
1999-03
Primary completion
1999-07
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject FIGOPITANT Small molecule 0.1 mg Oral
Subject FIGOPITANT Small molecule 25 mg Oral

Indications

No indication recorded.