Regeneron's Casirivimab and Imdevimab Receive the US FDA's EUA as the First Combination Therapy for COVID-19
Shots:
- The US FDA has issued a EUA for casirivimab (1-200mg) + imdevimab (1-200mg) administered together for mild to mod. COVID-19 in adults and pediatric patients aged ≥12yrs. weighing at least 40kg [~88 pounds]) with positive results of direct SARS-CoV-2 viral testing and who are at high risk for progressing to severe COVID-19
- The EUA is based on a P-II study that showed a reduction in hospitalization or ER visits in patients at high risk for disease progression within 28days after treatment and a reduction in viral loads
- Initial doses of Ab cocktail will be made available to ~300-000 patients- with no medication out-of-pocket costs- under the US government allocation program
Ref: Regeneron | Image: Fox Business
Click here to read the full press release
This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com