June 9th 2023
Findings from the phase 3 PhALLCON trial show that ponatinib plus reduced-intensity chemotherapy could be a new standard of care for patients with Philadelphia chromosome–positive acute lymphoblastic leukemia.
February 27th 2023
Ponatinib/Blinatumomab Combo Shows Promising Efficacy and Safety in Ph+ ALL
January 20th 2023Phase 2 study shows ponatinib and blinatumomab to represent a promising chemotherapy-free, hematopoietic stem cell transplant–sparing treatment for patients with Philadelphia chromosome–positive acute lymphocytic leukemia.
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FDA Grants Breakthrough Therapy Designation to SNDX-5613 for R/R KMT2Ar Acute Leukemia
December 6th 2022Based on phase 1 data of the AUGMENT-101 trial, the FDA has granted a breakthrough therapy designation to SNDX-5613 for patients with relapsed or refractory KMT2A rearranged acute leukemia.
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Study of Ponatinib Versus Imatinib Meets Primary End Point in Ph+ ALL
November 30th 2022Takeda Pharmaceuticals announced that the phase 3 PhALLCON trial of ponatinib for Philadelphia-positive acute lymphoblastic leukemia succeeded in improving the rate of minimal residual disease–negative complete remission.
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Managing Patients in the Changing Treatment Landscape of ALL
November 21st 2022In an interview with Targeted Oncology, Mark R. Litzow, MD, discussed managing patients with different subtypes of ALL and the session he was a part of during the National Comprehensive Cancer Network 2022 Annual Congress: Hematologic Malignancies.
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Over 50% of Patients With R/R Acute Leukemias Respond to SNDX-5613 in AUGMENT-101
November 4th 2022Updated data from the phase 1/2 AUGMENT trial led to a 30% complete remission rate and an overall response rate of 53% with SNDX-5613 when used in patients with relapsed/refractory acute leukemias.
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Recent Updates in Diagnosing and Treating Acute Lymphoblastic Leukemia
October 11th 2022In an interview with Targeted Oncology, Kjeld Schmiegelow, MD provided a deep dive into his SOHO 2022 presentation as well as the other acute lymphoblastic leukemia discussions presented during the session.
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