Having suffered a setback last year when deficiencies at a third-party manufacturer scuppered hopes of a quick US approval of sutimlimab for cold agglutinin disease, Sanofi has released more promising data on its C1s inhibitor at the European Hematology Association meeting.
Seven months after a surprise rejection from regulators in the US, Sanofi has presented new late-stage data on its rare blood disorder drug sutimlimab which will provide the basis for a submission in Europe and a resubmission Stateside in the coming months.
The French giant has presented data at the European Hematology Association meeting on sutimlimab from a second Phase III study...
The oral BTK inhibitor impresses in a Phase II trial for IgG4-related disease.
The $1.25bn buyout is a simple deal for BioNTech, bringing new mRNA R&D and manufacturing capacity while also ending a bothersome patent dispute.
Will Zydus’s acquisition and licensing deal with Agenus turn out to be a strategic move towards building an oncology portfolio or an opportunistic one driven by a venture capital mindset?
