Clinical trial
A Phase 2 Randomized Double-blind Placebo-controlled Study To Evaluate The Efficacy And Safety Of Adjunctive Recombinant Human Plasma Gelsolin With Standard Care For Moderate-to-Severe ARDS Due To Pneumonia Or Other Infections
NCT05947955 is registered in ClinicalTrials.gov with BioAegis Therapeutics Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 2 Randomized Double-blind Placebo-controlled Study To Evaluate The Efficacy And Safety Of Adjunctive Recombinant Human Plasma Gelsolin With Standard Care For Moderate-to-Severe ARDS Due To Pneumonia Or Other Infections
- Lead sponsor
- BioAegis Therapeutics Inc.
- Phase
- Phase 2
- Overall status
- Recruiting
- Start date
- October 3, 2024
- Completion date
- March 1, 2028
- Enrollment
- 600 (estimated)
- Sites
- 70
Conditions
As the registry lists them; a condition with its own page is linked.
acute respiratory distress syndrome, infections