Genmab — Juli 2019
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ok
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The news of the approval was clearly a surprise to investors, sending Karyopharm's stock shooting up about 40%. The FDA's final decision is at odds with that of the Oncologic Drug's Advisory Committee (ODAC), which had voted 8-5 against recommending approval and instead advocated waiting for results from the ongoing Phase III BOSTON trial.
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The FDA granted accelerated approval to Karyopharm's application for Xpovio (selinexor) as a treatment for multiple myeloma (MM) in patients refractory to at least two proteasome inhibitors, two immunomodulators, and an anti-CD38 monoclonal antibody
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At Medwatch skriver som de gør er fint nok - der er trods alt andre der læser med end os investorer, så når der er tale om dødelige bivirkninger, så må og skal det ud til alle. De skriver også at Janssen har udsendt deres materiale her i slutningen af Juni......hvem ved måske i forbindelse med MAIA godkendelsen.
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God morgen.
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