drugset / Trial / NCT01611311
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Rising Doses of BI 409306
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | OSORESNONTRINE | Small molecule | 25 mg | Oral |
| Subject | OSORESNONTRINE | Small molecule | 50 mg | Oral |
Indications
No indication recorded.