drugset / Trial / NCT04366050

Ramipril for the Treatment of COVID-19

NCT04366050

Phase 2 Completed 160 enrolled University of California, San Diego Pfizer · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

In this study we propose to treat 560 patients with ramipril or placebo for 14 days. After an initial evaluation for COVID-19 status, medical history, and symptom assessment, patients will receive either 2.5 mg/day of ramipril or placebo. Patients' symptoms and study endpoints will be monitored at regular intervals. After 14 days, patients will undergo a laboratory assessment and an end-of-treatment follow-up visit at day 28. The primary endpoints of successful therapy will be improved survival, reductions in ICU admissions, and/or reductions in use of mechanical ventilator support.

Timeline

Start
2020-05-11
Primary completion
2021-05-12
Completion
2021-05-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramipril Small molecule 2.5 mg Oral

Indications