Sanofi and Regeneron have announced that EU regulators have agreed to review Dupixent for asthma and cemiplimab for advanced cutaneous squamous cell carcinoma. The French pharmaceutical company is seeking approval for Dupixent as an supplementary maintenance treatment in certain adults and adolescents, aged 12 years old and higher, with inadequately controlled moderate-to-severe asthma. The drug
Sanofi and Regeneron have announced varied fortunes for their cancer drug Zaltrap, with the drug gaining a quick evaluation in the USA for colorectal cancer, but failing in a late-stage prostate cancer clinical trial. Sanofi announced today that the US Food and Drug Administration (FDA)Â has granted priority review of the Biologics License Application for
Regeneron Pharmaceuticals and EUSA Pharma have announced that US regulators have approved their blindness drug and leukaemia therapy, respectively. The US FDA (Food and Drug Administration) has given the okay to Regeneron’s Eylea, also known as VEGF Trap-Eye, for the treatment of patients with wet age-related Macular Degeneration at a recommended dose of 2 milligrams
