Pfizer no longer plans to read out an interim analysis on its Duchenne muscular dystrophy gene therapy program by the end of the year, it disclosed at an investor event last week. Instead, the pharma company plans to wait for the final analysis.
The Phase III study for fordadistrogene movaparvovec is expected to be completed in April, according to the federal clinical trials database. In October, Pfizer had guided that there could be an interim analysis at year-end and a final analysis in the second half of 2024.
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