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 7, 2024, Applied 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 furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.
The information provided in this Form 8-K, including Exhibit 99.1 hereto, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any of the Company’s filings under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits: |
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The following exhibit is attached with this current report on Form 8-K:
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Exhibit |
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Description |
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99.1 |
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104 |
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Cover Page Interactive Data File - the cover page iXBRL tags are embedded within the inline XBRL document. |
SIGNATURE
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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APPLIED THERAPEUTICS, INC. |
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Dated: November 7, 2024 |
By: |
/s/ Shoshana Shendelman |
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Name: |
Shoshana Shendelman |
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Title: |
President and Chief Executive Officer |
Exhibit 99.1
Applied Therapeutics Reports Third Quarter 2024 Financial Results
NEW YORK, November 7, 2024 – Applied Therapeutics, Inc. (Nasdaq: APLT) (the “Company”), a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need, today reported financial results for the third quarter ended September 30, 2024.
“We are proud of the significant progress we’ve made this quarter as we prepare for a transformational year ahead, with a focus on transitioning from a clinical-stage company to a commercial organization. With regulatory submissions for govorestat underway in two rare disease indications of urgent unmet need, Classic Galactosemia and SORD Deficiency, we continue to thoughtfully execute our pre-launch initiatives,” said Shoshana Shendelman, PhD, Founder and CEO of Applied Therapeutics. “As we approach the final stages of the NDA review process for Classic Galactosemia in parallel with a near-term NDA submission for SORD Deficiency, we remain confident in the promise of govorestat and its ability to address the underlying mechanisms of both diseases. We look forward to the opportunity to bring govorestat to patients in 2025.”
Recent Highlights
Financial Results
About Applied Therapeutics
Applied Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of novel drug candidates against validated molecular targets in indications of high unmet medical need. The Company’s lead drug candidate, govorestat, is a novel central nervous system penetrant Aldose Reductase Inhibitor
(ARI) for the treatment of CNS rare metabolic diseases, including Galactosemia, SORD Deficiency, and PMM2-CDG. The Company is also developing AT-001, a novel potent ARI, for the treatment of Diabetic Cardiomyopathy, or DbCM, a fatal fibrosis of the heart. The preclinical pipeline also includes AT-003, an ARI designed to cross through the back of the eye when dosed orally, for the treatment of Diabetic retinopathy.
To learn more, please visit www.appliedtherapeutics.com and follow the company on Twitter @Applied_Tx.
Forward-Looking Statements
This press release contains “forward-looking statements” that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, included in this press release regarding the strategy, future operations, prospects, plans and objectives of management, including words such as “may,” “will,” “expect,” “anticipate,” “plan,” “intend,” “predicts” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are forward-looking statements. These include, without limitation, statements regarding the (i) likelihood that the Company’s ongoing NDA and MMA submissions will be approved and the timing of any decision and (ii) statements related to the scheduling or timing of any potential FDA or EMA meetings, interactions or submissions. Forward-looking statements in this release involve substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by the forward-looking statements, and we, therefore cannot assure you that our plans, intentions, expectations or strategies will be attained or achieved.
Such risks and uncertainties include, without limitation, (i) our plans to develop, market and commercialize our product candidates, (ii) the initiation, timing, progress and results of our current and future preclinical studies and clinical trials and our research and development programs, (iii) our ability to take advantage of expedited regulatory pathways for any of our product candidates, (iv) our estimates regarding expenses, future revenue, capital requirements and needs for additional financing, (v) our ability to successfully acquire or license additional product candidates on reasonable terms and advance product candidates into, and successfully complete, clinical studies, (vi) our ability to maintain and establish collaborations or obtain additional funding, (vii) our ability to obtain and timing of regulatory approval of our current and future product candidates, (viii) the anticipated indications for our product candidates, if approved, (ix) our expectations regarding the potential market size and the rate and degree of market acceptance of such product candidates, (x) our ability to fund our working capital requirements and expectations regarding the sufficiency of our capital resources, (xi) the implementation of our business model and strategic plans for our business and product candidates, (xii) our intellectual property position and the duration of our patent rights, (xiii) developments or disputes concerning our intellectual property or other proprietary rights, (xiv) our expectations regarding government and third-party payor coverage and reimbursement, (xv) our ability to compete in the markets we serve, (xvi) the impact of government laws and regulations and liabilities thereunder, (xvii) developments relating to our competitors and our industry, (xviii) our ability to achieve the anticipated benefits from the agreements entered into in connection with our partnership with Advanz Pharma and (xiv) other factors that may impact our financial results. In light of the significant uncertainties in these forward-looking statements, you should not rely upon forward-looking statements as predictions of future events. Although we believe that we have a reasonable basis for each forward-looking statement contained in this press release, we cannot guarantee that the future results, levels of activity, performance or events and circumstances reflected in the forward-looking statements will be achieved or occur at all. Factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in our filings with the U.S. Securities and Exchange Commission, including the “Risk Factors”
contained therein. Except as otherwise required by law, we disclaim any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events or circumstances or otherwise.
Contacts
Investors:
Julie Seidel/Andrew Vulis
646-970-0543
appliedtherapeutics@argotpartners.com
Media:
media@appliedtherapeutics.com
Applied Therapeutics, Inc.
Condensed Balance Sheets
(in thousands, except share and per share data)
(Unaudited)
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As of |
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As of |
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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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$ |
98,867 |
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$ |
49,898 |
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Security deposits and leasehold improvements |
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253 |
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254 |
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Prepaid expenses and other current assets |
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5,483 |
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4,234 |
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Total current assets |
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104,603 |
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54,386 |
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Operating lease right-of-use asset |
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1,963 |
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447 |
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TOTAL ASSETS |
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$ |
106,566 |
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$ |
54,833 |
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LIABILITIES AND STOCKHOLDERS’ EQUITY/(DEFICIT) |
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CURRENT LIABILITIES: |
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Current portion of operating lease liabilities |
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$ |
264 |
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$ |
429 |
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Accounts payable |
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2,837 |
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1,742 |
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Accrued expenses and other current liabilities |
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13,489 |
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15,286 |
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Warrant liabilities |
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82,377 |
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53,725 |
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Total current liabilities |
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98,967 |
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71,182 |
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NONCURRENT LIABILITIES: |
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Noncurrent portion of operating lease liabilities |
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1,707 |
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38 |
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Clinical holdback - long-term portion |
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— |
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759 |
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Total noncurrent liabilities |
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1,707 |
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797 |
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Total liabilities |
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100,674 |
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71,979 |
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STOCKHOLDERS’ EQUITY/(DEFICIT): |
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Common stock, $0.0001 par value; 250,000,000 shares authorized as of September 30, 2024 and 200,000,000 shares authorized as of December 31, 2023; 116,356,474 shares issued and outstanding as of September 30, 2024 and 84,869,832 shares issued and outstanding as of December 31, 2023 |
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11 |
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8 |
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Preferred stock, par value $0.0001; 10,000,000 shares authorized as of September 30, 2024 and December 31, 2023; 0 shares issued and outstanding as of September 30, 2024 and December 31, 2023 |
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— |
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— |
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Additional paid-in capital |
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624,098 |
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451,432 |
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Accumulated deficit |
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(618,217 |
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(468,586 |
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Total stockholders' equity/(deficit) |
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5,892 |
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(17,146 |
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TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY/(DEFICIT) |
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$ |
106,566 |
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$ |
54,833 |
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Applied Therapeutics, Inc.
Condensed Statements of Operations
(in thousands, except share and per share data)
(Unaudited)
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Three Months Ended |
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Nine Months Ended |
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September 30, |
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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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License revenue |
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$ |
— |
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$ |
— |
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$ |
— |
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$ |
10,660 |
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Research and development services revenue |
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122 |
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— |
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455 |
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— |
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Total revenue |
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122 |
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— |
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455 |
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10,660 |
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COSTS AND EXPENSES: |
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Research and development |
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14,828 |
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10,785 |
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37,049 |
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38,602 |
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General and administrative |
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15,037 |
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4,710 |
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34,683 |
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15,585 |
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Total costs and expenses |
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29,865 |
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15,495 |
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71,732 |
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54,187 |
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LOSS FROM OPERATIONS |
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(29,743 |
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(15,495 |
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(71,277 |
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(43,527 |
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OTHER (EXPENSE) INCOME, NET: |
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Interest income |
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1,357 |
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392 |
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2,572 |
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1,020 |
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Change in fair value of warrant liabilities |
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(40,184 |
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(27,277 |
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(80,845 |
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(39,611 |
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Other (expense) income, net |
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(21 |
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10 |
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(81 |
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34 |
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Total other expense, net |
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(38,848 |
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(26,875 |
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(78,354 |
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(38,557 |
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Net loss |
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$ |
(68,591 |
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$ |
(42,370 |
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$ |
(149,631 |
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$ |
(82,084 |
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Net loss per share attributable to common stockholders |
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$ |
(0.48 |
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$ |
(0.47 |
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$ |
(1.09 |
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$ |
(1.09 |
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Weighted-average common stock outstanding |
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144,345,781 |
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90,669,969 |
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137,893,249 |
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75,482,234 |
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