- Phase 2 Trial of Stenoparib Concluded Early due to Clear Clinical Benefits Achieved
- On Track to Regain Compliance with All Nasdaq Listing Requirements
-
- Warrant Overhang Near Elimination
- Allarity Withdraws its Form S-1
- Establishes Equity of
- Cash Balance of
"The start of 2024 has been a pivotal period for
First Quarter 2024 and Recent Operational Highlights
Allarity Therapeutics now has a single class of shares after investor-initiated conversions of all outstanding Series A Preferred Stock and the majority of warrants into common stock. Significantly, all variable-priced warrants have been exercised, reducing market overhang from warrants. A limited number of fixed-price warrants remain unexercised, each with an exercise price of$20 . Additionally, the Company has fully repaid all bridge notes. These developments simplify Allarity's capital structure, enhancing the attractiveness of its stock. As of today, the total number of shares is 17,606,739.- Allarity has requested the
SEC to withdraw its Form S-1 registration, reflecting its improved financial outlook. - Stockholders' equity at Allarity significantly exceeds the
$2.5 million minimum required by Nasdaq under Listing Rule 5550(b)(1) due to the fact that the Company has a cash balance of$14 million , reduced its debts and increased its equity to$15 million utilizing an "At-The-Market” (ATM) offering under a Form S-3. This method was the most rapid and cost-effective way to raise capital before theMay 14, 2024 , deadline set by Nasdaq. Formal confirmation by Nasdaq of regaining compliance with Rule 5550(b)(1) is being sought. - The Company has concluded its Phase 2 clinical trial of stenoparib early due to clear clinical benefits observed, including tumor shrinkage and long-term disease stability, in heavily pre-treated ovarian cancer patients. Using Allarity’s DRP® companion diagnostic to pre-screen patients, the trial targeted those most likely to benefit. The promising results have provided sufficient proof of concept, prompting Allarity to halt enrollment with the purpose of preparing a follow-on trial with FDA regulatory intent. The company plans to outline further details in a clinical update.
- Allarity has regained compliance with Nasdaq’s Listing Rule 5550(a)(2), which mandates a minimum bid price of
$1.00 , after executing a reverse stock split onApril 9, 2024 . Following the split, the company's stock maintained a closing bid price above$1.00 for more than ten consecutive trading days, leading to a confirmation from Nasdaq of compliance. - Driven by promising Phase 2 trial data, Allarity has strategically shifted its focus solely to accelerating the development of stenoparib for targeting advanced, recurrent ovarian cancer. This shift has allowed significant reductions in ongoing costs and better alignment with new strategic priorities while deprioritizing other projects like the development of IXEMPRA® and dovitinib.
- Allarity received an extension until
April 24, 2024 , from theNasdaq Hearings Panel to meet listing requirements, including maintaining a minimum$1.00 share price and increasing stockholders' equity to$2.5 million . The extension was granted following the Company's presentation of a comprehensive plan to regain compliance. - CEO
Thomas Jensen presented Allarity Therapeutics’ development of the DRP® platform for personalized cancer therapy at the Biomarkers 2024 conference, focusing on its use in a phase 2 study of stenoparib for ovarian cancer. The presentation took place onFebruary 29, 2024 , inLondon, UK .
First Quarter 2024 Operating Results
R&D Expenses: Research and Development (R&D) expenses for the quarter ended
G&A Expenses: General and Administrative (G&A) expenses for the quarter ended
Net Loss from Operations: Net Loss from Operations for the quarter ended
Net Loss: Net loss was
About the Drug Response Predictor – DRP® Companion Diagnostic
Allarity uses its drug-specific DRP® to select those patients who, by the gene expression signature of their cancer, are found to have a high likelihood of benefiting from a specific drug. By screening patients before treatment, and only treating those patients with a sufficiently high, drug-specific DRP score, the therapeutic benefit rate may be significantly increased. The DRP method builds on the comparison of sensitive vs. resistant human cancer cell lines, including transcriptomic information from cell lines combined with clinical tumor biology filters and prior clinical trial outcomes. DRP is based on messenger RNA expression profiles from patient biopsies. The DRP® platform has proven its ability to provide a statistically significant prediction of the clinical outcome from drug treatment in cancer patients dozens of clinical studies (both retrospective and prospective). The DRP platform, which can be used in all cancer types and is patented for more than 70 anti-cancer drugs, has been extensively published in the peer-reviewed literature.
About
Follow Allarity on Social Media
LinkedIn: https://www.linkedin.com/company/allaritytx/
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Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements provide the Company’s current expectations or forecasts of future events. The words “anticipates,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predicts,” “project,” “should,” “would” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. These forward-looking statements include, but are not limited to, the impact of recent financial and operational achievements on future quarterly performance, potential future financings, and the anticipated regulatory progress of stenoparib following the final outcome of our Phase 2 clinical trial. Any forward-looking statements in this press release are based on management’s current expectations of future events and are subject to multiple risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to the risks associated with maintaining compliance with Nasdaq's continued listing requirements, obtaining regulatory approval for stenoparib, and potential market fluctuations that could impact our financial stability and the drug's market entry. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in our Form S-1 registration statement filed on
CONDENSED CONSOLIDATED BALANCE SHEETS
(
2024 | 2023 | |||||||
(Unaudited) | ||||||||
ASSETS | ||||||||
Current assets: | ||||||||
Cash | $ | 312 | $ | 166 | ||||
Other current assets | 110 | 209 | ||||||
Prepaid expenses | 542 | 781 | ||||||
Tax credit receivable | 1,331 | 815 | ||||||
Total current assets | 2,295 | 1,971 | ||||||
Non-current assets: | ||||||||
Property, plant and equipment, net | 18 | 20 | ||||||
Intangible assets | 9,656 | 9,871 | ||||||
Total assets | $ | 11,969 | $ | 11,862 | ||||
LIABILITIES AND STOCKHOLDERS’ (DEFICIT) EQUITY | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 11,058 | $ | 8,416 | ||||
Accrued liabilities | 1,553 | 1,309 | ||||||
Warrant derivative liability | 2,664 | 3,083 | ||||||
Income taxes payable | 43 | 59 | ||||||
Convertible promissory notes and accrued interest, net of debt discount | 2,690 | 1,300 | ||||||
Total current liabilities | 18,008 | 14,167 | ||||||
Non-current liabilities: | ||||||||
Deferred tax | 432 | 446 | ||||||
Total liabilities | 18,440 | 14,613 | ||||||
Commitments and contingencies (Note 16) | ||||||||
Stockholders’ (deficit) equity | ||||||||
Series A Preferred stock | 1,510 | 1,742 | ||||||
Common stock, | — | — | ||||||
Additional paid-in capital | 90,699 | 90,369 | ||||||
Accumulated other comprehensive loss | (386 | ) | (411 | ) | ||||
Accumulated deficit | (98,294 | ) | (94,451 | ) | ||||
Total stockholders’ deficit | (6,471 | ) | (2,751 | ) | ||||
Total liabilities, preferred stock and stockholders’ (deficit) equity | $ | 11,969 | $ | 11,862 |
All common share data has been retroactively adjusted to effect the reverse stock split in 2024. |
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(Unaudited)
(
Three months ended | ||||||||
2024 | 2023 | |||||||
Operating expenses: | ||||||||
Research and development | $ | 2,170 | $ | 1,427 | ||||
General and administrative | 2,070 | 2,241 | ||||||
Total operating expenses | 4,240 | 3,668 | ||||||
Loss from operations | (4,240 | ) | (3,668 | ) | ||||
Other income (expenses) | ||||||||
Interest income | — | 4 | ||||||
Interest expense | (102 | ) | (92 | ) | ||||
Foreign exchange gains | 76 | 95 | ||||||
Change in fair value adjustment of derivative and warrant liabilities | 419 | 309 | ||||||
Net other income | 393 | 316 | ||||||
Net loss for the period before tax benefit | (3,847 | ) | (3,352 | ) | ||||
Income tax benefit | 4 | — | ||||||
Net loss | (3,843 | ) | (3,352 | ) | ||||
Deemed dividend of 5% on Series C Convertible Preferred stock | — | (4 | ) | |||||
Gain on extinguishment of Series A Convertible Preferred stock | 191 | — | ||||||
Deemed dividend on Series A Convertible Preferred stock | (228 | ) | — | |||||
Net loss attributable to common stockholders | $ | (3,880 | ) | $ | (3,356 | ) | ||
Basic and diluted net loss per common stock | $ | (22.14 | ) | $ | (6,356.06 | ) | ||
Weighted-average number of common stock outstanding, basic and diluted | 175,266 | 528 | ||||||
Other comprehensive loss, net of tax: | ||||||||
Net loss | $ | (3,843 | ) | $ | (3,352 | ) | ||
Change in cumulative translation adjustment | 25 | 84 | ||||||
Total comprehensive loss attributable to common stockholders | $ | (3,818 | ) | $ | (3,268 | ) |
All common share data has been retroactively adjusted to effect the reverse stock split in 2024. |
###
Company Contact:
investorrelations@allarity.com
Media Contact:
Thomas Pedersen
Carrotize PR & Communications
+45 6062 9390
tsp@carrotize.com
Attachment
- Allarity Therapeutics Press Release - Allarity Therapeutics Reports First Quarter Financial Results
Source:
2024 GlobeNewswire, Inc., source