drugset / Trial / NCT03224325
A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Escalating Multiple Doses of TAK-831 in Healthy Participants
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate the safety and tolerability of TAK-831 when administered as multiple oral doses at escalating dose levels in healthy participants.
Timeline
- Start
- 2017-07-21
- Primary completion
- 2018-09-09
- Completion
- 2018-09-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Luvadaxistat | Small molecule | 15 mg | Oral |
| Subject | Luvadaxistat | Small molecule | 100 mg | Oral |
| Subject | Luvadaxistat | Small molecule | 300 mg | Oral |
| Subject | Luvadaxistat | Small molecule | 600 mg | Oral |
| Subject | Luvadaxistat | Small molecule | 800 mg | Oral |
| Subject | Luvadaxistat | Small molecule | 1200 mg | Oral |
Indications
No indication recorded.