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ESH translational research conferences cover cutting-edge biological, therapeutic and clinical questions. The ESH CLL conference program consists of leading-edge basic and clinical science with a panel of global experts in the field who provided numerous formal and informal discussions to address the present and the future of CLL research.
🎥 This #WorldLeukemiaDay watch @zucenka (@VU_LT) discuss data from a study investigating venetoclax combinations in FLT3- and IDH1-mutated acute myeloid #Leukemia:
As it's #WorldLeukemiaDay, why not listen to our recent podcast episode on the sequencing of BTKi therapy in CLL, which focuses on treatment considerations and emerging strategies.🩸
Click here to check it out:
🎧 https://ow.ly/8J5y50ZAsJV
🚨 The FDA approves ropeginterferon alfa-2b for the treatment of essential thrombocythemia!
This approval introduces the first new FDA-approved treatment for ET in nearly 3 decades, offering a long-acting interferon-based approach supported by durable response and hematologic
🧬 AAV gene therapy in hemophilia: what comes next?
Hear @RKaczmarekDr discuss the challenges of current AAV-based approaches, including durability, liver toxicity, and potential malignancy risks, alongside emerging non-AAV strategies.
ESH translational research conferences cover cutting-edge biological, therapeutic and clinical questions. The ESH CLL conference program consists of leading-edge basic and clinical science with a panel of global experts in the field who provided numerous formal and informal discussions to address the present and the future of CLL research.
🎥 This #WorldLeukemiaDay watch @zucenka (@VU_LT) discuss data from a study investigating venetoclax combinations in FLT3- and IDH1-mutated acute myeloid #Leukemia:
As it's #WorldLeukemiaDay, why not listen to our recent podcast episode on the sequencing of BTKi therapy in CLL, which focuses on treatment considerations and emerging strategies.🩸
Click here to check it out:
🎧 https://ow.ly/8J5y50ZAsJV
🚨 The FDA approves ropeginterferon alfa-2b for the treatment of essential thrombocythemia!
This approval introduces the first new FDA-approved treatment for ET in nearly 3 decades, offering a long-acting interferon-based approach supported by durable response and hematologic
🧬 AAV gene therapy in hemophilia: what comes next?
Hear @RKaczmarekDr discuss the challenges of current AAV-based approaches, including durability, liver toxicity, and potential malignancy risks, alongside emerging non-AAV strategies.
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