Full Press Release Details
-- On track to submit supplemental new drug application for AYVAKIT® (avapritinib) in non-advanced SM in Q4 2022, with an anticipated U.S. launch in mid-2023 --
-- Reports updated data from the SYMPHONY trial of BLU-945 demonstrating clinical activity and a differentiated safety profile, supporting combination development in first-line EGFR-mutant non-small cell lung cancer --
-- Expects to achieve the high-end of total revenue guidance of $180 million to $200 million for full-year 2022 --
-- Blueprint Medicines to webcast Investor Day 2022 event today at 8:30 a.m. ET --
"In addition, today we are reaffirming total revenue guidance for full-year 2022, while we lower product revenue guidance based on performance in the third quarter and our near-term expectations for growth. Over the last year, we have established AYVAKIT as the standard of care in patients who are being actively treated for their advanced SM, and we are now focusing on increasing treatment rates in patients with SM and an associated hematologic neoplasm, where there has been lower adoption. In parallel, we are prioritizing efforts to bring AYVAKIT to patients with non-advanced SM, which, if approved, would represent a 15-fold or larger opportunity based on the number of patients with moderate-to-severe non-advanced SM who are diagnosed, being treated for their SM, and observable in U.S. claims data today."
2027 Blueprint Global Business Strategy
Blueprint Medicines aims to achieve the following by the end of 2027:
Investor Day Presentation Highlights
At the Investor Day event, Blueprint Medicines plans to:
Third Quarter 2022 Highlights and Recent Progress
AYVAKIT®/AYVAKYT® (avapritinib): SM and PDGFRA gastrointestinal stromal tumor
GAVRETO® (pralsetinib): RET-altered cancers
BLU-945, BLU-701, BLU-525, and BLU-451: EGFR-mutant NSCLC
Key Upcoming Milestones
Blueprint Medicines expects to achieve the following near-term milestones:
Third Quarter 2022 Results
Financial Guidance
Blueprint Medicines anticipates it will achieve the high end of previously provided revenue guidance for full-year 2022 of approximately $180 million to $200 million , including approximately $108 million to $111 million in AYVAKIT net product revenues. The company continues to expect that its existing cash, cash equivalents and investments, together with anticipated future product revenues, will provide sufficient capital to enable the company to achieve a self-sustainable financial profile.
Conference Call Information
Blueprint Medicines will host a live conference call and webcast at 8:30 a.m. ET today for Investor Day and to discuss third quarter 2022 financial results. The live webcast of the event will be available under "Events and Presentations" in the Investors & Media section of Blueprint Medicines' website at http://ir.blueprintmedicines.com/ . A replay of the webcast will be archived on Blueprint Medicines' website for 90 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, strategies, timelines and expectations for interactions with the FDA and other regulatory authorities; to submit a supplemental New Drug Application to the FDA for AYVAKIT in non-advanced SM, with a subsequent submission of a type II variation marketing authorization application to the European Medicines Agency; plans and timing for presenting detailed data from the PIONEER trial of AYVAKIT in patients with non-advanced SM, and, expectations regarding the potential benefits of AYVAKIT in treating patients with non-advanced SM; statements regarding plans and expectations for Blueprint Medicines' current or future approved drugs and drug candidates; the potential benefits of any of Blueprint Medicines' current or future approved drugs or drug candidates in treating patients; and Blueprint Medicines' financial performance, strategy, goals and anticipated milestones, business plans and focus. The words "aim," "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 impact of the COVID-19 pandemic to Blueprint Medicines' business, operations, strategy, goals and anticipated milestones, including Blueprint Medicines' ongoing and planned research and discovery activities, ability to conduct ongoing and planned clinical trials, clinical supply of current or future drug candidates, commercial supply of current or future approved products, and launching, marketing and selling current or future approved products; Blueprint Medicines' ability and plans in continuing to establish and expand a commercial infrastructure, and successfully launching, marketing and selling current or future approved products; Blueprint Medicines' ability to successfully expand the approved indications for AYVAKIT/AYVAKYT and GAVRETO or obtain marketing approval for AYVAKIT/AYVAKYT in additional geographies in the future; the delay of any current or planned clinical trials or the development of Blueprint Medicines' current or future drug candidates; 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 either as monotherapies or in combination with other agents or may impact the anticipated timing of data or regulatory submissions; the timing of the initiation of clinical trials and trial cohorts at clinical trial sites and patient enrollment rates; actions of regulatory agencies, which may affect the initiation, timing and progress of clinical trials; Blueprint Medicines' ability to obtain, maintain and enforce patent and other intellectual property protection for AYVAKIT/AYVAKYT, GAVRETO or any drug candidates it is developing; Blueprint Medicines' ability to develop and commercialize companion diagnostic tests for AYVAKIT/AYVAKYT, GAVRETO or any of its current and future drug candidates; Blueprint Medicines' ability to successfully expand its operations, research platform and portfolio of therapeutic candidates, and the timing and costs thereof; Blueprint Medicines' ability to realize the anticipated benefits of its executive leadership transition plan; and the success of Blueprint Medicines' current and future collaborations, financing arrangements, partnerships or licensing arrangements. These and other risks and uncertainties are described in greater detail in the section entitled "Risk Factors" in Blueprint Medicines' filings with the Securities and Exchange Commission (SEC), including Blueprint Medicines' most recent Annual Report on Form 10-K, as supplemented by its most recent Quarterly Report on Form 10-Q 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.
Blueprint Medicines, AYVAKIT, AYVAKYT, GAVRETO and associated logos are trademarks of Blueprint Medicines Corporation.
| Blueprint Medicines Corporation | ||||||
| Selected Condensed Consolidated Balance Sheet Data | ||||||
| (in thousands) | ||||||
| (unaudited) | ||||||
| September 30, | December 31, | |||||
| 2022 | 2021 | |||||
| Cash, cash equivalents and investments | $ | 1,192,640 | $ | 1,034,643 | ||
| Working capital (1) | 1,052,155 | 404,260 | ||||
| Total assets | 1,458,392 | 1,252,225 | ||||
| Deferred revenue (2) | 16,624 | 36,576 | ||||
| Liability related to the sale of future royalties and revenues (2) | 423,653 | - | ||||
| Term loan (2) | 138,350 | - | ||||
| Total liabilities | 818,085 | 281,490 | ||||
| Total stockholders' equity | 640,307 | 970,735 | ||||
| (1) Blueprint defines working capital as current assets less current liabilities. (2) Includes both current and long-term portions of the balance |
| Blueprint Medicines Corporation | |||||||||||
| Condensed Consolidated Statements of Operations Data | |||||||||||
| (in thousands, except per share data) | |||||||||||
| (unaudited) | |||||||||||
| Three Months Ended, September 30 | Nine Months Ended, September 30 | ||||||||||
| 2022 | 2021 | 2022 | 2021 | ||||||||
| Revenues: | |||||||||||
| Product revenue, net | $ | 28,634 | $ | 17,270 | $ | 80,929 | $ | 37,658 | |||
| Collaboration and license revenue | 9,843 | 6,918 | 56,826 | 35,401 | |||||||
| License revenue - Related Party | 27,500 | - | 27,500 | - | |||||||
| Total revenues | 65,977 | 24,188 | 165,255 | 73,059 | |||||||
| Cost and operating expenses: | |||||||||||
| Cost of sales | 3,000 | 3,790 | 12,965 | 10,385 | |||||||
| Collaboration loss sharing | 1,665 | 3,269 | 7,076 | 3,269 | |||||||
| Research and development | 127,981 | 84,419 | 359,579 | 244,157 | |||||||
| Selling, general and administrative | 57,608 | 49,806 | 173,354 | 141,093 | |||||||
| Total cost and operating expenses | $ | 190,254 | 141,284 | 552,974 | 398,904 | ||||||
| Other income (expense): | |||||||||||
| Interest income (expense), net | (8,396) | 552 | (7,527) | 1,923 | |||||||
| Other income (expense), net | 396 | (522) | 575 | (1,109) | |||||||
| Total other income (expense) | $ | (8,000) | 30 | (6,952) | 814 | ||||||
| Loss before income taxes | $ | (132,277) | (117,066) | (394,671) | (325,031) | ||||||
| Income tax expense | (886) | (175) | (4,200) | (368) | |||||||
| Net loss | $ | (133,163) | $ | (117,241) | $ | (398,871) | $ | (325,399) | |||
| Net loss per share — basic and diluted | $ | (2.23) | $ | (2.00) | $ | (6.70) | $ | (5.58) | |||
| Weighted-average number of common shares used in net loss per share — basic and diluted | 59,758 | 58,647 | 59,564 | 58,361 |
SOURCE Blueprint Medicines Corporation