drugset / Trial / NCT02706834
Safety, Tolerability and Pharmacokinetics of Escalating Single Doses of TAK-828 in Healthy Participants
RandomizedCrossoverQuadruple-blindOther
Summary
The purpose of this study is to evaluate the safety and tolerability of single oral doses of TAK-828 in healthy non-Japanese and Japanese participants.
Timeline
- Start
- 2016-03-01
- Primary completion
- 2016-06-17
- Completion
- 2016-06-17
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TAK-828 | Unknown | 0.1 mg | Oral |
| Subject | TAK-828 | Unknown | 0.5 mg | Oral |
| Subject | TAK-828 | Unknown | 3 mg | Oral |
| Subject | TAK-828 | Unknown | 15 mg | Oral |
| Subject | TAK-828 | Unknown | 50 mg | Oral |
| Subject | TAK-828 | Unknown | 100 mg | Oral |
| Subject | TAK-828 | Unknown | 150 mg | Oral |
| Subject | TAK-828 | Unknown | 200 mg | Oral |
Indications
No indication recorded.