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
XTANDI becomes the first and only androgen receptor signaling inhibitor approved for use with or without a GnRH analog therapy in nonmetastatic castration-sensitive prostate cancer
Proposed combination enhances Pfizer’s position as a leading company in oncology
Submissions based on favorable MagnetisMM-3 trial results in patients with relapsed or refractory multiple myeloma
Data show 37% reduction in risk of disease progression or death in men with metastatic castration-resistant prostate cancer treated with TALZENNA plus XTANDI
Study achieves primary endpoint of radiographic progression-free survival
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