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Clinical Trial Summary

This master protocol serves as a common reference for the inpatient and outpatient clinical studies that share common elements.


Clinical Trial Description

There are currently two addenda to this master protocol: Addendum 1, Study LDOS-21-001-01, is a Phase 2, randomized, single-blind, placebo-controlled study to evaluate the safety and efficacy of the combination of famotidine and celecoxib as a treatment in moderate-to-severe patients hospitalized for COVID-19. Addendum 2, Study LDOS-21-001-02, is a Phase 2 randomized, placebo-controlled, double-blind study to evaluate the safety and efficacy of the combination of famotidine and celecoxib as a post-exposure prophylaxis (PEP) for newly infected COVID-19 patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05077332
Study type Interventional
Source Leidos Life Sciences
Contact
Status Active, not recruiting
Phase Phase 2
Start date December 29, 2021
Completion date January 2025

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