Full Press Release Details
At the 2019 American Society of Clinical Oncology (ASCO) Annual Meeting and 24 th Congress of the European Hematology Association (EHA), Blueprint Medicines plans to present:
The accepted abstracts are listed below and are now available online on the ASCO and EHA conference websites, respectively: https://am.asco.org/ and https://ehaweb.org/congress/eha24/key-information/ .
2019 American Society of Clinical Oncology (ASCO) Annual Meeting May 31-June 4, 2019 ; Chicago, Illinois
Oral Presentation
Presentation Title: Clinical activity and tolerability of BLU-667, a highly potent and selective RET inhibitor, in patients (pts) with advanced RET-fusion+ non-small cell lung cancer (NSCLC) Session Title: Lung Cancer—Non-Small Cell Metastatic Session Date & Time: Monday, June 3, 2019 from 8:00 a.m. – 11:00 a.m. CT ( 9:00 a.m. – 12:00 p.m. ET ) Abstract Number: 9008
Poster Discussion Presentations
Presentation Title: Activity and tolerability of BLU-667, a highly potent and selective RET inhibitor, in patients with advanced RET-altered thyroid cancers Session Title: Head and Neck Cancer Poster Session Date & Time: Saturday, June 1, 2019 from 1:15 p.m. – 4:15 p.m. CT ( 2:15 p.m. – 5:15 p.m. ET ) Poster Discussion Session Date & Time: Saturday, June 1, 2019 from 4:30 – 6:00 p.m. CT ( 5:30 p.m. – 7:00 p.m. ET ) Abstract Number : 6018
Presentation Title: Clinical activity of avapritinib in ≥ fourth line (4L+) and PDGFRA Exon 18 gastrointestinal stromal tumors (GIST) Session Title : Sarcoma Poster Session Date & Time : Saturday, June 1, 2019 from 8:00 a.m. – 11:00 a.m. CT ( 9:00 a.m. – 12:00 p.m. ET ) Poster Discussion Session Date & Time: Saturday, June 1, 2019 from 3:00 p.m. – 4:30 p.m. CT ( 4:00 p.m. – 5:30 p.m. ET ) Abstract Number : 11022
24 th Congress of the European Hematology Association (EHA) June 13-16, 2019 ; Amsterdam, The Netherlands
Oral Presentation
Presentation Title: Avapritinib, a potent and selective inhibitor of KIT D816V, induces complete and durable responses in patients (pts) with advanced systemic mastocytosis (AdvSM) Session Title: New Agents in MPN Presentation Date & Time : Saturday, June 15, 2019 from 12:00 p.m. – 12:15 p.m. CEST ( 6:00 a.m. – 6:15 a.m. ET ) Abstract Number : S830
Investor Event and Webcast Information
Blueprint Medicines will host an investor event on Monday, June 3, 2019 beginning at 6:30 p.m. CT ( 7:30 p.m. ET ) in Chicago to provide a portfolio update, including a review of updated clinical data from the ongoing ARROW trial of BLU-667 in patients with RET-altered cancers and the ongoing registration-enabling NAVIGATOR trial in patients with PDGFRA Exon 18 mutant and fourth-line GIST. The event will be webcast live and can be accessed under the "Investors & Media—Events & Presentations" section of Blueprint Medicines' website at www.BlueprintMedicines.com . A replay of the webcast will be available approximately two hours after the event and will be available for 30 days following the event.
About Blueprint Medicines
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, statements regarding plans and timelines for submitting marketing applications for avapritinib and BLU-667 in the United States and Europe , including expectations related to the data for such submissions; and Blueprint Medicines' strategy, goals and anticipated milestones, business plans and focus. The words "may," "will," "could," "would," "should," "expect," "plan," "anticipate," "intend," "believe," "estimate," "predict," "project," "potential," "continue," "target" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks and uncertainties related to the delay of any current or planned clinical trials or the development of Blueprint Medicines' drug candidates, including avapritinib, BLU-667, BLU-554 and BLU-782; Blueprint Medicines' advancement of multiple early-stage efforts; Blueprint Medicines' ability to successfully demonstrate the safety and efficacy of its drug candidates and gain approval of its drug candidates on a timely basis, if at all; the preclinical and clinical results for Blueprint Medicines' drug candidates, which may not support further development of such drug candidates; actions of regulatory agencies, which may affect the initiation, timing and progress of clinical trials; Blueprint Medicines' ability to develop and commercialize companion diagnostic tests for its current and future drug candidates; and the success of Blueprint Medicines' current and future collaborations, including its cancer immunotherapy collaboration with F. Hoffmann-La Roche Ltd and Hoffmann-La Roche Inc. and its collaboration with CStone Pharmaceuticals. These and other risks and uncertainties are described in greater detail in the section entitled "Risk Factors" in Blueprint Medicines' Quarterly Report on Form 10-Q for the period ended March 31, 2019 , as filed with the Securities and Exchange Commission (SEC) on May 9, 2019 , and any other filings that Blueprint Medicines has made or may make with the SEC in the future. Any forward-looking statements contained in this press release represent Blueprint Medicines' views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date. Except as required by law, Blueprint Medicines explicitly disclaims any obligation to update any forward-looking statements.
SOURCE Blueprint Medicines Corporation