March 5th 2025
The investigational immunotherapy bexmarilimab has been granted orphan drug designation from the FDA for patients with myelodysplastic syndromes.
February 21st 2025
Moving Beyond JAK Inhibition for the Treatment of Myelofibrosis
October 18th 2023Aaron T. Gerds, MD, MS, discusses available treatment options for patients with myelofibrosis and some of the agents that are currently under development, inching toward regulatory approval in the field of myelofibrosis.
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Primary Myelofibrosis Outcomes Could Be Affected by Socio-Racial Factors
September 8th 2023At the SOHO 2023 Annual Meeting, Mohammad Bakri Hammami, MD, spoke about the need to address disparities related to race, sex, and age among patients with primary myelofibrosis to ensure that everyone receives high-quality treatment.
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Goals of Managing Cytopenic Myelofibrosis in Younger Patients
August 29th 2023During a Targeted Oncology™ Case-Based Roundtable™ event, Naveen Pemmaraju, MD, and participants discussed the role of JAK inhibitors in managing myelofibrosis particularly in younger patients who may receive allogeneic stem cell transplant. This is the first of 2 articles based on this event.
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EXCEED-ET Investigates an Alternative Option for Disease Modification in Essential Thrombocytopenia
July 16th 2023In an interview with Targeted Oncology, Lucia Masarova, MD, discussed the ongoing EXCEED-ET clinical trial and its potential to provide a new option to alter disease and ward off post-essential thrombocytopenia myelofibrosis in adult patients.
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