drugset / Trial / NCT07208591

To Evaluate The Safety and Efficacy of STSA-1002 Injection in Patients With Acute Respiratory Distress Syndrome

NCT07208591 ↗

Phase 3 Recruiting 406 enrolled Staidson (Beijing) Biopharmaceuticals Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy, safety and tolerability of STSA-1002 injection in patients with acute respiratory distress syndrome

Timeline

Start
2025-10-31
Primary completion
2026-07
Completion
2026-10

Drugs

EvaluationDrugModalityDoseRoute
Subject GREZIPRUBART Monoclonal antibody — Intravenous