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Myeloma Combination Cuts Line for FDA Approval After Strong ASH Results
The FDA granted a priority voucher and fast-tracked review for teclistamab plus daratumumab after the MajesTEC-3 trial showed an 83% risk reduction in progression or death.
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Myeloma Combination Cuts Line for FDA Approval After Strong ASH Results
(MedPage Today) -- Under a program designed to accelerate the approval of products that could address key national priorities, the FDA said it proactively awarded a national priority voucher to teclistamab (Tecvayli) in combination with daratumumab...
·New York, United States
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