drugset / Trial / NCT01611311

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Rising Doses of BI 409306

NCT01611311

Phase 1 Completed 40 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the current study is to investigate the safety and tolerability of BI 409306 in healthy young and elderly male and female volunteers following oral administration of repeated rising doses, given once daily over 14 days to young healthy genotyped and elderly healthy male/female volunteers.

Timeline

Start
2012-05-01
Primary completion
2012-08-01
Completion
2012-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject OSORESNONTRINE Small molecule 25 mg Oral
Subject OSORESNONTRINE Small molecule 50 mg Oral

Indications

No indication recorded.