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NCT05238532

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

Withdrawn Phase 1 Last updated 4 April 2023
What this trial tests

Phase 1 trial testing CT303 in Acute Respiratory Distress Syndrome. Withdrawn.

Timeline
26 January 2022
Primary endpoint
22 February 2023
22 February 2023

Quick facts

Lead sponsorGC Cell Corporation
PhasePhase 1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date26 January 2022
Primary completion22 February 2023
Estimated completion22 February 2023
Sites3 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

GC Cell Corporation — full company profile →

Who can join

19 and older, any sex, with Acute Respiratory Distress Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of CT303

Trials testing the same drug.

Other recruiting trials for Acute Respiratory Distress Syndrome

Currently open trials in the same condition.

Other GC Cell Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05238532.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing