drugset / Trial / NCT05085197

The Safety and Tolerability of STSA-1005 Following Intravenous Infusion in Healthy Subjects

NCT05085197 ↗

Phase 1 Completed 32 enrolled Staidson Biopharma Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This was a single ascending dose, randomized, double-blind study assessing the safety, tolerability and pharmacokinetics of STSA-1005 in healthy participants. Four kinds different doses and dose-matched placebo were administered under fasted conditions.

Timeline

Start
2021-10-27
Primary completion
2022-04-05
Completion
2022-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject STSA-1005 Unknown 1 mg/kg Intravenous
Subject STSA-1005 Unknown 2.5 mg/kg Intravenous
Subject STSA-1005 Unknown 5 mg/kg Intravenous
Subject STSA-1005 Unknown 10 mg/kg Intravenous

Indications

No indication recorded.