A Duchenne muscular dystrophy patient died of cardiac arrest on Friday in a Phase 2 trial of Pfizer’s gene therapy, the pharma company confirmed.
The patient received fordadistrogene movaparvovec in early 2023 as part of Pfizer’s DAYLIGHT study enrolling patients 2 and 3 years old. As a result of the boy’s death, Pfizer is pausing dosing in the crossover portion of its Phase 3 CIFFREO study in patients 4 to 7 years old.
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