drugset / Trial / NCT03870555
A Study to Investigate the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of TAK-954 in Healthy Adult Participants
RandomizedCrossoverDouble-blindOther
Summary
The purpose of this study is to evaluate the safety, tolerability, and PK of single ascending intravenous doses of TAK-954.
Timeline
- Start
- 2019-03-08
- Primary completion
- 2019-05-16
- Completion
- 2019-05-16
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | felcisetrag | Small molecule | 0.1 mg | Intravenous |
| Subject | felcisetrag | Small molecule | 0.5 mg | Intravenous |
| Subject | felcisetrag | Small molecule | 1 mg | Intravenous |
| Subject | felcisetrag | Small molecule | 2 mg | Intravenous |
Indications
No indication recorded.