Stoke Therapeutics, Inc 8-K, filed Nov 5, 2024
Stoke Therapeutics, Inc. (STOK)
About this 8-K
Stoke Therapeutics, Inc filed this 8-K on November 5, 2024.
Items reported
- Item 2.02: Financial results
- Item 9.01: Financial statements and exhibits
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
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Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
Securities registered pursuant to Section 12(b) of the Act:
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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
Item 2.02 Results of Operations and Financial Condition.
On November 5, 2024, Stoke Therapeutics, Inc. (the “Company”) issued a press release announcing its financial results for the quarter ended September 30, 2024. A copy of the press release is attached as Exhibit 99.1 to this report.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit Number |
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Description |
99.1 |
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104 |
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Cover Page Interactive Data File (embedded within the Inline XBRL document) |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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STOKE THERAPEUTICS, INC. |
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Date: |
November 5, 2024 |
By: |
/s/ Thomas E. Leggett |
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Thomas E. Leggett |
EX-99.1
Stoke Therapeutics Reports Third Quarter Financial Results and Provides Business Updates
– Company plans to provide seizure as well as cognition and behavior data from all patients treated with initial 70mg doses followed by 45mg maintenance dosing in studies of zorevunersen by year-end –
– Discussions with FDA and global regulatory agencies related to a single global Phase 3 study of zorevunersen continue to progress; Company to provide an update by year-end –
– As of September 30, 2024, Company had $269.2 million in cash, cash equivalents, and marketable securities –
BEDFORD, Mass., November 5, 2024 – Stoke Therapeutics, Inc. (Nasdaq: STOK), a biotechnology company dedicated to restoring protein expression by harnessing the body’s potential with RNA medicine, today reported financial results for the third quarter of 2024 and provided business updates including those related to zorevunersen, the Company’s proprietary antisense oligonucleotide (ASO) which is in development by Stoke as the first potential medicine to address the genetic cause of Dravet syndrome.
“We are headed into a busy year-end as we prepare to share new data which is representative of our proposed Phase 3 dosing regimen and complete our regulatory discussions toward alignment on that study design,” said Edward M. Kaye, M.D., Chief Executive Officer of Stoke Therapeutics. “Key to our regulatory discussions are the assessments of behavior and cognition in patients with Dravet syndrome. In our studies of zorevunersen, we have demonstrated substantial and sustained effects across multiple measures of disease, starting within the first year of treatment. These data give us confidence in our Phase 3 planning and the potential for zorevunersen to go beyond seizure management by addressing the root cause of the disease.”
The Company announced today that it has submitted abstracts for presentation at the American Epilepsy Society meeting taking place December 6-10, in Los Angeles, California. Included among these planned presentations are new data from all patients treated in the clinical studies with initial 70mg doses followed by 45mg maintenance dosing in studies of zorevunersen. A Phase 3 regimen of two or three loading doses of 70mg followed by maintenance doses of 45mg is currently under discussion with global regulatory agencies. As the Company continues to focus on zorevunersen as its lead program, it will delay the start of the Phase 1 study of STK-002, its clinical candidate for the treatment of autosomal dominant optic atrophy (ADOA).
Recent Program Highlights and Upcoming Milestones
Third Quarter 2024 Financial Results
Year-to-Date 2024 Financial Results
About Dravet Syndrome
Dravet syndrome is a severe and progressive genetic epilepsy characterized by frequent, prolonged and refractory seizures, beginning within the first year of life. Dravet syndrome is difficult to treat and has a poor long-term prognosis. Complications of the disease often
contribute to a poor quality of life for patients and their caregivers. The effects of the disease go beyond seizures and often include intellectual disability, developmental delays, movement and balance issues, language and speech disturbances, growth defects, sleep abnormalities, disruptions of the autonomic nervous system and mood disorders. The disease is classified as a developmental and epileptic encephalopathy due to the developmental delays and cognitive impairment associated with the disease. Compared with the general epilepsy population, people living with Dravet syndrome have a higher risk of sudden unexpected death in epilepsy, or SUDEP. There are no approved disease-modifying therapies for people living with Dravet syndrome. One out of 16,000 babies are born with Dravet syndrome, which is not concentrated in a particular geographic area or ethnic group.
About Zorevunersen (STK-001)
Zorevunersen is an investigational new medicine for the treatment of Dravet syndrome currently being evaluated in ongoing clinical trials. Stoke believes that zorevunersen, a proprietary antisense oligonucleotide (ASO), has the potential to be the first disease-modifying therapy to address the genetic cause of Dravet syndrome. Zorevunersen is designed to upregulate Nav1.1 protein expression by leveraging the non-mutant (wild-type) copy of the SCN1A gene to restore physiological Nav1.1 levels, thereby reducing both occurrence of seizures and significant non-seizure comorbidities. Zorevunersen has been granted orphan drug designation by the FDA and the EMA, and rare pediatric disease designation by the FDA as a potential new treatment for Dravet syndrome.
About Stoke Therapeutics
Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body’s potential with RNA medicine. Using Stoke’s proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore protein levels. Stoke’s first compound, zorevunersen (STK-001), is in clinical testing for the treatment of Dravet syndrome, a severe and progressive genetic epilepsy. Dravet syndrome is one of many diseases caused by a haploinsufficiency, in which a loss of ~50% of normal protein levels leads to disease. Stoke is pursuing the development of STK-002 for the treatment of autosomal dominant optic atrophy (ADOA), the most common inherited optic nerve disorder. Stoke’s initial focus is haploinsufficiencies and diseases of the central nervous system and the eye, although proof of concept has been demonstrated in other organs, tissues, and systems, supporting its belief in the broad potential for its proprietary approach. Stoke is headquartered in Bedford, Massachusetts with offices in Cambridge, Massachusetts. For more information, visit https://www.stoketherapeutics.com/.
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: the Company’s current or future financial position and liquidity; the ability of zorevunersen (STK-001) to treat the underlying causes of Dravet syndrome and reduce seizures or show improvements in behavior and cognition at the indicated dosing levels or at all; and the timing
and expected progress of clinical trials, data readouts, regulatory meetings, regulatory decisions and other presentations. Statements including words such as “expect,” “plan,” “will,” “continue,” 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 prove incorrect or do not fully materialize, could cause our results to differ materially from those expressed or implied by such forward-looking statements, including, but not limited to, risks and uncertainties related to: the Company’s ability to advance, obtain regulatory approval of, and ultimately commercialize its product candidates, including zorevunersen; the timing of data readouts and interim and final results of preclinical and clinical trials; the receipt and timing of potential regulatory decisions; positive results in a clinical trial may not be replicated in subsequent trials or successes in early stage clinical trials may not be predictive of results in later stage trials; the Company’s ability to fund development activities and achieve development goals, including expectations regarding its collaboration with Acadia Pharmaceuticals; the Company’s ability to protect its intellectual property; the direct or indirect impact of global business, political and macroeconomic conditions, including inflation, interest rate volatility, cybersecurity events, uncertainty with respect to the federal budget, instability in the global banking system and volatile market conditions, and global events, including public health crises, and ongoing geopolitical conflicts, such as the conflicts in Ukraine and the Middle East; and other risks and uncertainties described under the heading “Risk Factors” in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023, its quarterly reports on Form 10-Q, and the other documents it files from time to time with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release, and the Company undertakes no obligation to revise or update any forward-looking statements to reflect events or circumstances after the date hereof.
Financial Tables Follow
Stoke Therapeutics, Inc. and subsidiary
Consolidated balance sheets
(in thousands, except share and per share amounts)
(unaudited)
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September 30, |
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December 31, |
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2024 |
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2023 |
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Assets |
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Current assets: |
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Cash and cash equivalents |
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$ |
150,016 |
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$ |
191,442 |
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Marketable securities - current |
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89,184 |
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9,952 |
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Prepaid expenses |
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9,837 |
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11,320 |
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Restricted cash - current |
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75 |
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— |
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Interest receivable |
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691 |
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64 |
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Other current assets |
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3,809 |
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2,561 |
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Total current assets |
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$ |
253,612 |
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$ |
215,339 |
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Marketable securities - long-term |
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29,952 |
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— |
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Restricted cash - long-term |
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494 |
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569 |
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Operating lease right-of-use assets |
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4,928 |
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6,611 |
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Property and equipment, net |
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4,333 |
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5,823 |
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Total assets |
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$ |
293,319 |
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$ |
228,342 |
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Liabilities and stockholders’ equity |
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Current liabilities: |
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Accounts payable |
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$ |
2,485 |
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$ |
1,695 |
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Accrued and other current liabilities |
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15,768 |
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13,815 |
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Deferred revenue - current portion |
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31,612 |
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15,309 |
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Total current liabilities |
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$ |
49,865 |
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$ |
30,819 |
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Deferred revenue - net of current portion |
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8,291 |
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33,074 |
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Other long term liabilities |
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3,050 |
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4,884 |
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Total long term liabilities |
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11,341 |
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37,958 |
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Total liabilities |
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$ |
61,206 |
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$ |
68,777 |
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Stockholders’ equity |
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Common stock, par value of $0.0001 per share; 300,000,000 shares authorized, 52,941,191 and 45,918,233 shares issued and outstanding as of September 30, 2024 and December 31, 2023, respectively |
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5 |
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5 |
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Additional paid-in capital |
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712,290 |
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561,433 |
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Accumulated other comprehensive income (loss) |
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166 |
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(24 |
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Accumulated deficit |
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(480,348 |
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(401,849 |
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Total stockholders’ equity |
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$ |
232,113 |
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$ |
159,565 |
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Total liabilities and stockholders’ equity |
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$ |
293,319 |
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$ |
228,342 |
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Stoke Therapeutics, Inc. and subsidiary
Consolidated statements of operations and comprehensive loss
(in thousands, except share and per share amounts)
(unaudited)
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Three Months Ended September 30, |
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Nine Months Ended September 30, |
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2024 |
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2023 |
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2024 |
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2023 |
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Revenue |
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$ |
4,894 |
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$ |
3,308 |
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$ |
13,941 |
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$ |
5,978 |
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Operating expenses: |
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Research and development |
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22,205 |
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20,271 |
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65,710 |
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60,453 |
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General and administrative |
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12,692 |
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10,271 |
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35,950 |
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30,712 |
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Total operating expenses |
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34,897 |
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30,542 |
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101,660 |
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91,165 |
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Loss from operations |
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(30,003 |
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(27,234 |
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(87,719 |
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(85,187 |
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Other income (expense): |
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Interest income (expense), net |
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3,545 |
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2,651 |
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9,668 |
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7,321 |
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Other income (expense), net |
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28 |
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41 |
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(448 |
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125 |
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Total other income (expense) |
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3,573 |
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2,692 |
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9,220 |
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7,446 |
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Net loss |
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$ |
(26,430 |
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$ |
(24,542 |
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$ |
(78,499 |
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$ |
(77,741 |
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Net loss per share, basic and diluted |
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$ |
(0.47 |
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$ |
(0.55 |
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$ |
(1.48 |
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$ |
(1.78 |
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Weighted-average common shares outstanding, basic |
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56,341,074 |
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44,266,017 |
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52,991,015 |
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43,669,987 |
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Comprehensive loss: |
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Net loss |
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$ |
(26,430 |
) |
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$ |
(24,542 |
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$ |
(78,499 |
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$ |
(77,741 |
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Other comprehensive gain: |
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Unrealized gain on marketable securities |
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181 |
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232 |
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190 |
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1,028 |
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Total other comprehensive gain |
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$ |
181 |
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$ |
232 |
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$ |
190 |
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$ |
1,028 |
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Comprehensive loss |
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$ |
(26,249 |
) |
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$ |
(24,310 |
) |
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$ |
(78,309 |
) |
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$ |
(76,713 |
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Stoke Media & Investor Contacts:
Dawn Kalmar
Chief Communications Officer
dkalmar@stoketherapeutics.com
781-303-8302
Doug Snow
Director, Communications & Investor Relations
IR@stoketherapeutics.com
508-642-6485