BRISBANE, Calif., Oct. 30, 2024 (GLOBE NEWSWIRE) -- Day One Biopharmaceuticals, Inc. (Nasdaq: DAWN) (“Day One” or the “Company”), a biopharmaceutical company dedicated to developing and commercializing targeted therapies for people of all ages with life-threatening diseases, today announced its third quarter 2024 financial results and highlighted recent corporate achievements.
“Our third quarter results demonstrate continued patient demand for OJEMDA, driven by the need for new therapies for children living with pediatric low-grade glioma,” said Jeremy Bender, Ph.D., chief executive officer of Day One. “Looking ahead to 2025, we plan to continue to drive growth by advancing our programs and pipeline, including DAY301, a potential first-in-class ADC targeting PTK7 that we expect to be in the clinic in the coming months.”
Program Highlights
Corporate Highlights and Upcoming Milestones
Third Quarter 2024 Financial Highlights
Upcoming Events
Conference Call
Day One will host a conference call and webcast today, October 30 at 4:30 p.m. Eastern Time. To access the live conference call by phone, dial 877-704-4453 (domestic) or 201-389-0920 (international), and provide the access code 13745150. Live audio webcast will be accessible from the Day One Investors & Media page. To ensure a timely connection to the webcast, it is recommended that participants register at least 15 minutes prior to the scheduled start time. An archived version of the webcast will be available for replay on the Events & Presentations section of the Day One Investors & Media page for 30 days following the event.
About OJEMDA™
OJEMDA (tovorafenib) is a Type II RAF kinase inhibitor of mutant BRAF V600, wild-type BRAF, and wild-type CRAF kinases.
OJEMDA is indicated for the treatment of patients 6 months of age and older with relapsed or refractory pediatric low-grade glioma (LGG) harboring a BRAF fusion or rearrangement, or BRAF V600 mutation. This indication is approved under accelerated approval based on response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).
Tovorafenib was granted Breakthrough Therapy and Rare Pediatric Disease designations by the FDA for the treatment of patients with pLGG harboring an activating RAF alteration, and it was evaluated by the FDA under priority review. Tovorafenib has also received Orphan Drug designation from the FDA for the treatment of malignant glioma and from the European Commission for the treatment of glioma.
For more information, please visit www.ojemda.com.
About Day One Biopharmaceuticals
Day One Biopharmaceuticals believes when it comes to pediatric cancer, we can do better. The Company was founded to address a critical unmet need: the dire lack of therapeutic development in pediatric cancer. Inspired by “The Day One Talk” that physicians have with patients and their families about an initial cancer diagnosis and treatment plan, Day One aims to re-envision cancer drug development and redefine what’s possible for all people living with cancer—regardless of age—starting from Day One.
Day One partners with leading clinical oncologists, families, and scientists to identify, acquire, and develop important targeted cancer treatments. The Company’s pipeline includes tovorafenib (OJEMDA™), DAY301 and a VRK1 inhibitor program.
Day One is based in Brisbane, California. For more information, please visit www.dayonebio.com or find the Company on LinkedIn or X.
Day One uses its Investor Relations website (ir.dayonebio.com), its X handle (x.com/DayOneBio), and LinkedIn Home Page (linkedin.com/company/dayonebio) as a means of disseminating or providing notification of, among other things, news or announcements regarding its business or financial performance, investor events, press releases, and earnings releases, and as a means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD.
Cautionary Note Regarding Forward-Looking Statements
This press release contains “forward-looking” statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to: Day One’s plans to develop and commercialize cancer therapies, expectations from current and planned clinical trials, the execution of the Phase 2 and Phase 3 clinical trial for tovorafenib as designed, expectations with respect to the timing of Day One’s Phase 1a/b clinical trial of DAY301, any expectations about safety, efficacy, timing and ability to complete clinical trials, release data results and to obtain regulatory approvals for tovorafenib and other candidates in development, and the ability of tovorafenib to treat pLGG or related indications.
Statements including words such as “believe,” “plan,” “continue,” “expect,” “will,” “develop,” “signal,” “potential,” or “ongoing” and statements in the future tense are forward-looking statements. These forward-looking statements involve risks and uncertainties, as well as assumptions, which, if they do not fully materialize or prove incorrect, could cause our results to differ materially from those expressed or implied by such forward-looking statements.
Forward-looking statements are subject to risks and uncertainties that may cause Day One’s actual activities or results to differ significantly from those expressed in any forward-looking statement, including risks and uncertainties in this press release and other risks set forth in our filings with the Securities and Exchange Commission, including Day One’s ability to develop, obtain and retain regulatory approval for or commercialize any product candidate, Day One’s ability to protect intellectual property, the potential impact of global business or macroeconomic conditions, including as a result of inflation, rising interest rates, instability in the global banking system, geopolitical conflicts and the sufficiency of Day One’s cash, cash equivalents and investments to fund its operations. These forward-looking statements speak only as of the date hereof and Day One specifically disclaims any obligation to update these forward-looking statements or reasons why actual results might differ, whether as a result of new information, future events or otherwise, except as required by law.
| Day One Biopharmaceuticals, Inc. Condensed Statements of Operations (in thousands, except share and per share amounts) (unaudited) | |||||||||||||||
| Three Months Ended September 30, | Nine Months Ended September 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Revenue: | |||||||||||||||
| Product revenue, net | $ | 20,070 | $ | — | $ | 28,262 | $ | — | |||||||
| License revenue | 73,691 | — | 73,691 | — | |||||||||||
| Total revenues | 93,761 | — | 101,953 | — | |||||||||||
| Cost and operating expenses: | |||||||||||||||
| Cost of product revenue | 1,590 | — | 2,297 | — | |||||||||||
| Research and development | 33,563 | 33,163 | 165,879 | 93,173 | |||||||||||
| Selling, general and administrative | 28,972 | 18,275 | 85,715 | 53,374 | |||||||||||
| Total cost and operating expenses | 64,125 | 51,438 | 253,891 | 146,547 | |||||||||||
| Income (loss) from operations | 29,636 | (51,438 | ) | (151,938 | ) | (146,547 | ) | ||||||||
| Non-operating income: | |||||||||||||||
| Gain from sale of priority review voucher | — | — | 108,000 | — | |||||||||||
| Investment income, net | 5,322 | 5,291 | 13,649 | 12,163 | |||||||||||
| Other income (expense), net | 1,197 | (3 | ) | 1,177 | (22 | ) | |||||||||
| Total non-operating income, net | 6,519 | 5,288 | 122,826 | 12,141 | |||||||||||
| Income (loss) before income taxes | 36,155 | (46,150 | ) | (29,112 | ) | (134,406 | ) | ||||||||
| Income tax benefit (expense) | 882 | — | (670 | ) | — | ||||||||||
| Net income (loss) | 37,037 | (46,150 | ) | (29,782 | ) | (134,406 | ) | ||||||||
| Net income (loss) per share - basic | $ | 0.38 | $ | (0.54 | ) | $ | (0.33 | ) | $ | (1.73 | ) | ||||
| Net income (loss) per share - diluted | $ | 0.38 | $ | (0.54 | ) | $ | (0.33 | ) | $ | (1.73 | ) | ||||
| Weighted-average number of common shares used in net income (loss) per share - basic | 96,623,123 | 85,952,501 | 90,164,895 | 77,682,237 | |||||||||||
| Weighted-average number of common shares used in net income (loss) per share - diluted | 96,937,759 | 85,952,501 | 90,164,895 | 77,682,237 | |||||||||||
| Day One Biopharmaceuticals, Inc. Selected Condensed Balance Sheet Data (in thousands) (unaudited) | |||||||
| September 30, 2024 | December 31, 2023 | ||||||
| Cash, cash equivalents and short-term investments | $ | 558,383 | $ | 366,347 | |||
| Total assets | 600,807 | 376,048 | |||||
| Total liabilities | 45,344 | 29,508 | |||||
| Accumulated deficit | (488,367 | ) | (458,585 | ) | |||
| Total stockholders’ equity | 555,463 | 346,540 | |||||
DAY ONE MEDIA
Laura Cooper, Head of Communications
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DAY ONE INVESTORS
LifeSci Advisors, PJ Kelleher
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| Last Trade: | US$13.44 |
| Daily Change: | -0.18 -1.32 |
| Daily Volume: | 535,046 |
| Market Cap: | US$1.320B |
July 30, 2024 May 06, 2024 | |
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