Daiichi Sankyo Co. Ltd.'s quizartinib has demonstrated an overall survival benefit as a single agent compared with chemotherapy in the pivotal QuANTUM-R study of relapsed/refractory acute myeloid leukemia patients with FLT3-ITD mutations, giving the company a potential foot in the door for the indication.
Daiichi's Phase III Quizartinib Data Pave Way In Niche AML Market
Showing an overall survival improvement in the especially hard to treat FLT3-ITD mutated patients is a significant achievement in AML, analysts say.
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Aldeyra’s dry eye candidate reproxalap received a second FDA complete response letter, but the firm expressed confidence about refiling quickly based on two ongoing studies.
Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
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