drugset / Trial / NCT05238532

Clinical Trial to Evaluate the Safety, Tolerability and Efficacy of CT303 in Patients With ARDS

NCT05238532 ↗

Phase 1 Withdrawn GC Cell Corporation
NaSingle-groupOpen-labelTreatment

Summary

Evaluate the safety, tolerability, efficacy and pharmacodynamics\&pharmacokinetic properties of CT303 in patients with ARDS.

Timeline

Start
2022-01-26
Primary completion
2023-02-22
Completion
2023-02-22

Outcome

Outcome not reported

Stopped (Enrollment): “Difficulties in recruiting Subjects”

Drugs

EvaluationDrugModalityDoseRoute
Subject CT303 Cell therapy 1e+06 cells/kg Intravenous
Subject CT303 Cell therapy 2e+06 cells/kg Intravenous