Pfizer suffers a DMD delay and halts BCMA trials amid safety woes
Pfizer has paused after seeing three cases of peripheral neuropathy in an early-stage study, enrollment in a critical analysis of its anti-BCMA bispecific antibody. Big Pharma shares news with details of delays to the start of the US part of Duchenne Muscular Dystrophy (DMD) Phase 3.
In February, Pfizer announced a crucial phase in the strength of the overall response rate of 80% seen in 20 patients treated with BCMA bispecific elanatamab, also known as PF-06863135, in Phase 1. 2 Incorporated into research. In a study of patients with relapsed and refractory multiple myeloma, Pfizer suspende...