drugset / Trial / NCT01371812
GSK2239633 FTIH Study
RandomizedCrossoverDouble-blindTreatment
Summary
The purpose of this first time into human study is to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK2239633 in healthy male subjects.
Timeline
- Start
- 2011-03-29
- Primary completion
- 2011-07-01
- Completion
- 2011-07-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GSK2239633 | Small molecule | 150 mg | Oral |
| Subject | GSK2239633 | Small molecule | 300 mg | Oral |
| Subject | GSK2239633 | Small molecule | 600 mg | Oral |
| Subject | GSK2239633 | Small molecule | 900 mg | Oral |
| Subject | GSK2239633 | Small molecule | 1200 mg | Oral |
| Subject | GSK2239633 | Small molecule | 1500 mg | Oral |