Invivoscribe is excited to announce that the LeukoStrat(R) CDx FLT3 Mutation Assay has been approved by the U.S. Food and Drug Administration (FDA) to aid in the selection of patients with newly diagnosed FLT3 -ITD positive acute myeloid leukemia (AML) who may be eligible to receive treatment with Daiichi Sankyo's VANFLYTA(R) (quizartinib). The LeukoStrat CDx FLT3 Mutation Assay identifies FLT3 -ITD positive AML patients who may be treated with this newly approved targeted therapy. US Intended