European Commission approves Pfizer’s Elrexfio for multiple myeloma
Conditional marketing authorization is based on clinically meaningful response rates, duration of response, and safety from the Phase 2 MagnetisMM-3 trial
Conditional marketing authorization is based on clinically meaningful response rates, duration of response, and safety from the Phase 2 MagnetisMM-3 trial
ELREXFIO’s label contains a boxed warning for cytokine release syndrome and neurologic toxicity
Columvi is part of Roche's industry-leading portfolio of T-cell engaging bispecific antibodies in non-Hodgkin lymphoma, which also includes the recently approved Lunsumio to treat follicular lymphoma
Once approved, Columvi will be the first CD20xCD3 T-cell-engaging bispecific antibody available to treat people in Europe with this aggressive lymphoma
The antiviral is efficacious in non-human primates, and is safe and well-tolerated in humans
Submissions based on favorable MagnetisMM-3 trial results in patients with relapsed or refractory multiple myeloma
According to GlobalData’s analyst consensus forecast, OTX-2002 is projected to have the highest revenue by 2028, with sales of $1.6 billion during that year
Patients receiving Polivy plus R-CHP for DLBCL reported similar health-related quality of life outcomes
AstraZeneca has acquired all outstanding equity of TeneoTwo in exchange for an upfront payment of $100m.
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