At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomized, Double-Blind, Comparative Trial of the Safety and Efficacy of Famotidine vs Placebo for the Treatment of Non-Hospitalized Symptomatic Adults With COVID-19
In Brief
A Phase 2 clinical trial evaluating Famotidine and Placebo for Covid-19. Completed, enrolled 56 participants across 1 site.
Detailed Summary
The overall objective of this study is to evaluate the clinical efficacy of oral famotidine in symptomatic non-hospitalized patients with confirmed COVID-19. This study is expected to enroll up to 84 patients with mild to moderate symptoms divided into each of the two study arms. Clinical outcomes of the two treatment arms will be compared. This study will be conducted virtually/remotely.
Study Details
Timeline
Arms & Interventions
Participants in this study arm will receive standard of care and prescribed famotidine at 80mg TID for a maximum of 14 days, or until hospital admission.
Participants in this study arm will receive standard of care and placebo for a maximum of 14 days.
Interventions
Standard or care treatment plus prescribed famotidine
Standard of care treatment plus placebo