Roche has secured its first regulatory approval for mosunetuzumab, a first-in-class CD20xCD3 bispecific antibody, as a treatment for patients with follicular lymphoma (FL) in the EU.
Roche is on the brink of its first regulatory approval for what could be the first bispecific antibody targeting CD3 and CD20 – mosunetuzumab – after getting a positive opinion for the drug
A subcutaneous formulation of MSD's top-selling cancer immunotherapy Keytruda was non-inferior to the current intravenous version in a head-to-head trial, setting up regulatory filings.