Blueprint: FDA Approves AYVAKIT as 1st and Only Treatment for Indolent Systemic Mastocytosis

 For the first time, patients with indolent SM have a medicine that treats the primary disease driver and is proven to provide broad and durable symptom relief --

-- Approval based on the positive PIONEER trial, in which once-daily AYVAKIT achieved significant improvements in disease symptoms and measures of mast cell burden, with a safety profile that compared favorably to placebo --

-- Blueprint Medicines to host investor conference call and webcast today at 4:30 p.m. ET --

Blueprint Medicines will host a live conference call and webcast today at 4:30 p.m. ET to discuss the FDA approval of AYVAKIT in ISM. The conference call may be accessed by dialing 833-470-1428 (domestic) or 404-975-4839 (international), and referring to conference ID 832860. A webcast of the call will also be available under "Events and Presentations" in the Investors & Media section of the Blueprint Medicines website at https://ir.blueprintmedicines.com/. The archived webcast will be available on the Blueprint Medicines website approximately two hours after the conference call and will be available for 30 days following the call.

https://finance.yahoo.com/news/fda-approves-ayvakit-avapritinib-first-200400327.html