Xpovio’s Solid Tumor Debut Faces Likely Three-Year Delay

Karyopharm will conduct another trial of the drug in p53 wild-type endometrial cancer after the FDA said SIENDO data were insufficient for approval.

Cancer
Karyopharm said the FDA told it during a meeting that topline trial results would not likely be sufficient for Xpovio's approval in endometrial cancer • Source: Shutterstock

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