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FDA Extends Review Period for Quizartinib for Adults With FLT3-ITD-Positive AML

Daiichi Sankyo announced that the new deadline for review of the application is July 24, 2023. ....

United States , Daiichi Sankyo , Mark Rutstein , Mikkael Sekeres , University Of Miami Health System , American Cancer Society , European Hematology Association Congress , Oncology Clinical Development , Prescription Drug User Fee Act , Risk Evaluation , Mitigation Strategies , American Cancer , Global Head , Hematology Association Congress , Sylvester Comprehensive Cancer Center , Miami Health System , Acute Myeloid Leukemia ,

FTC: E-commerce platform knowingly facilitated payments to scammers

Nexway, based in France, allegedly processed payments in its own name on behalf of a tech support scam and telemarketing company from 2016 to 2020. ....

United States , Casey Potenzone , Aaron Lazor , Brian Cotter , Victor Iezuitov , Tamas Kader , Polo Rocha , Better Business Bureau , Asknet Solutions , Department Of Justice , Deutsche Bank , Federal Trade Commission , Chief Strategic Officer Casey , Tech Live Connect , Tech Live , Hindustan Times , Live Connect , Premium Techie Support , Sensei Ventures , Federal Trade , Assured Money , Premium Tech Support , Card Fraud , Ab Technology ,

FDA Extends Review for Quizartinib in Newly Diagnosed FLT3-ITD+ AML

The FDA has extended the review period for a new drug application for quizartinib in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, and as continuation monotherapy following consolidation, for the treatment of newly diagnosed adult patients with FLT3-ITD–positive acute myeloid leukemia. ....

Mark Rutstein , Daiichi Sankyo , European Hematology Association Congress , Oncology Clinical Development At Daiichi Sankyo , Prescription Drug User Fee Act , Oncology Clinical Development , Hematology Association Congress , Acute Myeloid Leukemia , Flt3 Itd Positive Acute Myeloid Leukemia ,

Dr Andreeff on the Rationale for Investigating Uproleselan Plus Venetoclax and Azacitidine in AML

Michael Andreeff, MD, PhD, discusses the rationale for investigating uproleselan plus venetoclax and azacitidine in patients with acute myeloid leukemia.

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Dr Ball on Prior Research Supporting the SELECT-AML-1 Trial in Newly Diagnosed AML

Brian C. Ball, MD, discusses previous research on tamibarotene in newly diagnosed acute myeloid leukemia, and how these data support the ongoing phase 2 SELECT-AML-1 trial.

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