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The 8th World Congress on Controversies in Multiple Myeloma (COMy) took place from May 12 - 15 2022 in Paris, France, and virtually.
This meeting brought world experts together to discuss the latest controversies in multiple myeloma.
🎥 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.
The 8th World Congress on Controversies in Multiple Myeloma (COMy) took place from May 12 - 15 2022 in Paris, France, and virtually.
This meeting brought world experts together to discuss the latest controversies in multiple myeloma.
🎥 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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