drugset / Trial / NCT04425733
Frespaciguat (MK-5475) in Participants With Hypoxemia Due to COVID-19 Pneumonia (MK-5475-009)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Frespaciguat | Small molecule | 180 ug | Inhaled |
| Subject | Frespaciguat | Small molecule | 360 ug | Inhaled |