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Molnupiravir and COVID-19 Mortality Reduction in the Omicron Era
Sponsor: Charles University, Czech Republic
Summary
This retrospective real-world target trial emulation uses complete Czech nationwide registry data to evaluate whether molnupiravir treatment is associated with lower COVID-19 mortality during the Omicron era. The study compares adults with confirmed acute COVID-19 treated with molnupiravir in addition to standard care versus matched controls treated with standard care without molnupiravir. Patients are followed for three months from time zero, and primary endpoints are the COVID-19 case fatality rate and all-cause mortality.
Official title: Effect of Molnupiravir on COVID-19 Mortality in the Omicron Era: A Real-World Target Trial Emulation Using Complete Czech Nationwide Data
Key Details
Gender
All
Age Range
20 Years - Any
Study Type
OBSERVATIONAL
Enrollment
1814551
Start Date
2022-01-01
Completion Date
2024-12-31
Last Updated
2026-07-22
Healthy Volunteers
No
Conditions
Interventions
Molnupiravir
800 mg of molnupiravir administered twice daily, i.e., four capsules every 12 hours for five days.
Locations (1)
Department of Pharmacology, Third Faculty of Medicine, Charles University
Prague, Czechia