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Published on: November 5, 2021
Eua for Regen-Cov Now Includes COVID-19 Postexposure Prophylaxis.
1Diane S. Aschenbrenner is a former member of the faculty at Notre Dame of Maryland University and the Johns Hopkins University School of Nursing. She coordinates Drug Watch : diane.aschenbrenner@gmail.com .
REGEN-COV, a monoclonal antibody treatment, is now authorized for COVID-19 postexposure prophylaxis in high-risk individuals aged 12 and older. This treatment is not a replacement for COVID-19 vaccination.
Area of Science:
- Immunology
- Virology
- Public Health
Background:
- The COVID-19 pandemic necessitates effective prevention strategies.
- Monoclonal antibodies offer a targeted approach to viral infections.
- Identifying individuals at high risk for severe COVID-19 is crucial for intervention.
Purpose of the Study:
- To summarize the revised emergency use authorization for REGEN-COV.
- To outline the indication for REGEN-COV as postexposure prophylaxis.
- To clarify the target population for this preventive measure.
Main Methods:
- Review of the updated emergency use authorization (EUA) for REGEN-COV.
- Identification of the specific criteria for postexposure prophylaxis eligibility.
- Confirmation of the age and risk stratification for the intended population.
Main Results:
- REGEN-COV (casirivimab and imdevimab) is authorized for postexposure prophylaxis.
- The indication applies to adults and children aged 12+ at high risk of severe COVID-19.
- This prophylaxis is an adjunct to, not a substitute for, COVID-19 vaccination.
Conclusions:
- The revised EUA expands the utility of REGEN-COV for COVID-19 prevention.
- Postexposure prophylaxis with REGEN-COV provides an additional tool for high-risk populations.
- Vaccination remains the primary strategy for preventing COVID-19.
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