FDA accepts Bristol-Myers’ application for Opdivo+Yervoy regimen for advanced melanoma
The agency has granted priority review for this sBLA and is expected to respond by 30 September. The new application is based on data from CheckMate -069, the
Health innovation platform developer Aditxt and its fully owned subsidiary Ignite Proteomics have announced their plans for a business combination with a strategic partner that values the latter at an implied equity value of nearly $150m.
This is the first combination of BRAF/MEK inhibitors to demonstrate a statistically significant overall survival benefit for this patient population in two Phase III studies. Results are being
MM-398 is a new, stable nanotherapeutic encapsulation of the marketed chemotherapy drug irinotecan. The filing follows the recent submissions of NDA and marketing authorization application (MAA) by its