Karyopharm announces FDA approval of Xpovio (selinexor) as a treatment for patients with multiple myeloma after at least one prior therapy

Karyopharm Therapeutics

18 December 2020 - Oral Xpovio now available as a treatment option for patients with multiple myeloma as early as first relapse; significantly expands addressable patient population.

Karyopharm Therapeutics today announced that the U.S. FDA has approved Xpovio (selinexor), the Company's first-in-class, oral Selective Inhibitor of Nuclear Export medicine, in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

Read Karyopharm Therapeutics press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US