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

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
A Multi-center, Open-label Dose-escalation and Dose-finding Phase I Clinical Trial to Evaluate the Safety, Tolerability and Efficacy of CT303 in Patients With Acute Respiratory Distress Syndrome

Clinical Trial Summary

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

Clinical Trial Description

This study is a multi-center, open-label, dose-escalation and dose-finding phase 1 clinical trial. The primary purpose is to evaluate the safety and tolerability of CT303 and the Secondary purpose is to evaluate the efficacy of CT303 in patients with ARDS. And the exploratory purpose is to evaluate pharmacodynamics properties pharmacokinetic properties of CT303 in patients with ARDS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05238532
Study type Interventional
Source GC Cell Corporation
Contact
Status Withdrawn
Phase Phase 1
Start date January 26, 2022
Completion date February 22, 2023
View Details
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