Novartis’ Scemblix Receives Accelerated FDA Approval For Newly Diagnosed Ph+ CML In Adults
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(RTTNews) – Novartis (NVS) announced that Scemblix (asciminib) was granted accelerated approval by the US Food and Drug Administration for adult patients with newly diagnosed Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase or Ph+ CML-CP.
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