drugset / Trial / NCT04425733

Frespaciguat (MK-5475) in Participants With Hypoxemia Due to COVID-19 Pneumonia (MK-5475-009)

NCT04425733 ↗

Phase 1 Withdrawn Merck Sharp & Dohme LLC
RandomizedSequentialDouble-blindTreatment

Summary

The purpose of this study is to evaluate safety, tolerability, and pharmacodynamics of frespaciguat after administration of multiple doses to participants with COVID-19 pneumonia. The primary hypothesis is that frespaciguat when administered to participants with COVID-19 pneumonia and hypoxemia improves arterial oxygenation as measured by the ratio of blood oxygen saturation to fraction of inspired oxygen (SpO2/FiO2 ratio) compared to placebo.

Timeline

Start
2020-07-07
Primary completion
2020-11-10
Completion
2020-11-10

Outcome

Outcome not reported

Stopped (Business): “Business reasons”

Drugs

EvaluationDrugModalityDoseRoute
Subject Frespaciguat Small molecule 180 ug Inhaled
Subject Frespaciguat Small molecule 360 ug Inhaled

Indications