Clinical trial
A Phase 1/2/3 Adaptive Study to Evaluate the Safety, Tolerability, and Efficacy of REGN14256+Imdevimab for the Treatment of COVID-19 Patients Without Risk Factors for Progression to Severe Disease
NCT05081388 is registered in ClinicalTrials.gov with Regeneron Pharmaceuticals as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1/2/3 Adaptive Study to Evaluate the Safety, Tolerability, and Efficacy of REGN14256+Imdevimab for the Treatment of COVID-19 Patients Without Risk Factors for Progression to Severe Disease
- Lead sponsor
- Regeneron Pharmaceuticals
- Phase
- Phase 1/2
- Overall status
- Terminated
- Start date
- November 8, 2021
- Completion date
- June 30, 2022
- Enrollment
- 25 (actual)
- Sites
- 28
Conditions
As the registry lists them; a condition with its own page is linked.
sars-cov-2