drugset / Trial / NCT04818398

Study of Single-Ascending Doses of DS-6016a in Healthy Japanese Subjects

NCT04818398 ↗

Phase 1 Completed 48 enrolled Daiichi Sankyo
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

EvaluationDrugModalityDoseRoute
Subject PRAFNOSBART Monoclonal antibody — Subcutaneous