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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.

Summary by MedPage Today
(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...

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Anti-Aging, Acupuncture and Health News broke the news in on Monday, December 15, 2025.
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