Blueprint Medicines Corporation has announced the presentation of new data on the long-term clinical efficacy and safety profile of AYVAKIT®/AYVAKYT® (avapritinib) at the 2025 European Hematology Association (EHA2025) Hybrid Congress in Milan, Italy, and the European Academy of Allergy and Clinical Immunology (EAACI) Congress 2025 in Glasgow, United Kingdom. These presentations, including one oral and two flash talks, highlight Blueprint Medicines' ongoing efforts to improve treatment for patients with systemic mastocytosis $(SM)$. The data underscore AYVAKIT's role as a durable standard of care for both indolent and advanced SM, and emphasize the real-world burden of the disease. The findings are based on patient data from the PIONEER, PATHFINDER, and EXPLORER trials, with follow-up extending up to five years for indolent SM and 6.5 years for advanced SM. The data presentations are available on the company's website.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Blueprint Medicines Corporation published the original content used to generate this news brief via PR Newswire (Ref. ID: NE09480) on June 12, 2025, and is solely responsible for the information contained therein.
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