drugset / Trial / NCT02209714

Safety, Tolerability and Pharmacodynamics After Oral Administration of BIIF 1149 BS in Healthy Male Volunteers

NCT02209714 ↗

Phase 1 Completed 24 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of the study is to obtain information about the safety and tolerability of BIIF 1149 BS45 (single dose: 40, 65, 100 mg), to determine the pharmacologically active dose (range) by performing a citric acid challenge test and to obtain preliminary pharmacokinetic data.

Timeline

Start
1999-11
Primary completion
2000-02
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject FIGOPITANT Small molecule 40 mg Oral
Subject FIGOPITANT Small molecule 65 mg Oral
Subject FIGOPITANT Small molecule 100 mg Oral

Indications

No indication recorded.