drugset / Trial / NCT04818398
Study of Single-Ascending Doses of DS-6016a in Healthy Japanese Subjects
RandomizedParallel-groupTriple-blindTreatment
Summary
This study will assess the safety, tolerability, and pharmacokinetics of DS-6016a after subcutaneous injection in healthy Japanese participants.
Timeline
- Start
- 2021-04-01
- Primary completion
- 2021-12-24
- Completion
- 2022-07-26
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PRAFNOSBART | Monoclonal antibody | — | Subcutaneous |