Aprea Therapeutics Reports Third Quarter 2022 Financial Results and Provides Update on Business Operations
Aprea Therapeutics (Nasdaq: APRE) reported Q3 2022 financial results, highlighting a net loss of $4.0 million ($0.12 per share), a reduction from $9.5 million ($0.45 per share) in Q3 2021. As of September 30, 2022, cash and cash equivalents totaled $33.1 million, adequate to support operations through 2023. R&D expenses dropped significantly to $1.1 million from $6.0 million year-over-year. The company is advancing its ATRN-119 clinical trial for cancer treatment, with plans to open additional sites soon.
- The reduction in net loss to $4.0 million from $9.5 million year-over-year indicates improved financial management.
- Cash reserves of $33.1 million are projected to sustain operations through the end of 2023.
- Initiation of ATRN-119 Phase 1 clinical trial with plans to expand site enrollment.
- R&D expenses significantly decreased, indicating a potential slowdown in clinical advancements and pipeline development.
- Enrollment for APR-548 trial has been closed, suggesting challenges in patient recruitment or trial management.
BOSTON, Nov. 09, 2022 (GLOBE NEWSWIRE) -- Aprea Therapeutics, Inc. (Nasdaq: APRE), a biopharmaceutical company focused on developing and commercializing novel synthetic lethality-based cancer therapeutics targeting DNA damage response (DDR) pathways today reported financial results for the three and nine months ended September 30, 2022 and provided a business update.
“We are excited about the advancement of ATRN-119, the first macrocyclic ATR inhibitor, into clinical development,” said Oren Gilad, Ph.D., President and Chief Executive Officer of Aprea. “We look forward to collecting clinical data from our Phase 1 trial.”
Third Quarter Financial Results
- Cash and cash equivalents: As of September 30, 2022, the Company had
$33.1 million of cash and cash equivalents compared to$53.1 million of cash and cash equivalents as of December 31, 2021. The Company believes its cash and cash equivalents as of September 30, 2022 will be sufficient to meet its current projected operating requirements through the end of 2023. - Research and Development (R&D) expenses: R&D expenses were
$1.1 million for the quarter ended September 30, 2022, compared to$6.0 million for the comparable period in 2021. R&D expenses for the quarter ended September 30, 2022 primarily represented close out costs for (i) the Company’s pivotal Phase 3 clinical trial of eprenetapopt with azacitidine for the frontline treatment of TP53 mutant MDS, (ii) the Company’s Phase 2 post-transplant MDS/AML clinical trial, (iii) the Company’s Phase 1 AML trial, and (iv) the Company’s Phase 1/2 solid tumor trial and the Company’s Phase 1 dose-escalation trial of APR-548 as well as decreased non-cash stock-based compensation expense resulting from the acceleration of vesting of all outstanding stock options and restricted stock units in connection with the acquisition of Atrin in May 2022. - General and Administrative (G&A) expenses: G&A expenses were
$3.1 million for the quarter ended September 30, 2022, compared to$3.4 million for the comparable period in 2021. The decrease in G&A expenses was primarily due to decreased non-cash stock-based compensation expense resulting from the acceleration of vesting of all outstanding stock options and restricted stock units in connection with the acquisition of Atrin in May 2022, offset in part by increased professional fees. - Net loss: Net loss was
$4.0 million , or$0.12 per share for the quarter ended September 30, 2022, compared to a net loss of$9.5 million , or$0.45 per share for the quarter ended September 30, 2021. The Company had 52,237,885 shares of common stock outstanding as of September 30, 2022. The increased common stock outstanding resulted primarily from the conversion of 2,821,033 shares of Series A preferred stock into 28,210,330 shares of common stock during the third quarter of 2022.
Business Operations Update:
DDR Programs
ATRN-119 – ATRN-119 is an orally-bioavailable, highly potent and selective macrocyclic small molecule inhibitor of ATR, a protein with key roles in response to DNA damage. The Company is conducting a Phase 1 clinical trial to evaluate ATRN-119 monotherapy in cancer patients with defined genetic mutations. This trial was activated and opened for enrollment in the third quarter of 2022 and the Company expects to open 1-2 additional sites in the fourth quarter of 2022.
ATRN-W1051 – ATRN-W1051 is an orally-bioavailable, highly potent and selective small molecule inhibitor of WEE1, a key regulator of multiple phases of the cell cycle. ATRN-W1051 is currently in preclinical development and the Company anticipates commencing IND-enabling studies in the fourth quarter of 2022.
p53 Reactivator Programs
Eprenetapopt - APR-246, or eprenetapopt, is a small molecule p53 reactivator that has been tested in clinical trials for solid tumors and for hematologic malignancies. We currently have no ongoing clinical trials of eprenetapopt.
APR-548 - APR-548 is a second generation p53 reactivator that is being developed in an oral dosage form. We initiated a Phase 1 clinical trial testing APR-548 in relapsed/refractory MDS and AML and enrollment in the first dosing cohort was completed. There are currently no patients receiving APR-548 in this trial and enrollment into the trial has been closed.
About Aprea Therapeutics, Inc.
Aprea Therapeutics, Inc. is a biopharmaceutical company headquartered in Boston, Massachusetts with research facilities in Doylestown, Pennsylvania, focused on developing and commercializing novel cancer therapeutics that target DNA damage response pathways. The Company’s lead program is ATRN-119, an orally-bioavailable, highly potent and selective macrocyclic small molecule inhibitor of ATR, that is being tested in a Phase 1 clinical trial in solid tumor indications. ATRN-W1051, the Company’s novel WEE1 inhibitor, is in preclinical development. For more information, please visit the company website at www.aprea.com.
The Company may use, and intends to use, its investor relations website at https://ir.aprea.com/ as a means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD.
Forward Looking Statement
Certain information contained in this press release includes “forward-looking statements”, within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, related to our study analyses, clinical trials, regulatory submissions, and projected cash position. We may, in some cases use terms such as “future,” “predicts,” “believes,” “potential,” “continue,” “anticipates,” “estimates,” “expects,” “plans,” “intends,” “targeting,” “confidence,” “may,” “could,” “might,” “likely,” “will,” “should” or other words that convey uncertainty of the future events or outcomes to identify these forward-looking statements. Our forward-looking statements are based on current beliefs and expectations of our management team that involve risks, potential changes in circumstances, assumptions, and uncertainties. Any or all of the forward-looking statements may turn out to be wrong or be affected by inaccurate assumptions we might make or by known or unknown risks and uncertainties. These forward-looking statements are subject to risks and uncertainties including risks related to the success and timing of our clinical trials or other studies, risks associated with the coronavirus pandemic and the other risks set forth in our filings with the U.S. Securities and Exchange Commission. For all these reasons, actual results and developments could be materially different from those expressed in or implied by our forward-looking statements. You are cautioned not to place undue reliance on these forward-looking statements, which are made only as of the date of this press release. We undertake no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstances.
Source: Aprea Therapeutics, Inc.
Corporate Contacts:
Scott M. Coiante
Sr. Vice President and Chief Financial Officer
617-463-9385
Gregory A. Korbel
Sr. Vice President and Chief Operating Officer
617-463-9385
Aprea Therapeutics, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
September 30, 2022 | December 31, 2021 | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 33,112,601 | $ | 53,076,052 | |||
| Prepaid expenses and other current assets | 361,178 | 3,508,358 | |||||
| Total current assets | 33,473,779 | 56,584,410 | |||||
| Property and equipment, net | 12,237 | 23,870 | |||||
| Right of use lease and other noncurrent assets | 135,888 | 215,183 | |||||
| Total assets | $ | 33,621,904 | $ | 56,823,463 | |||
| Liabilities and Stockholders’ Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 1,136,064 | $ | 1,773,032 | |||
| Accrued expenses | 2,751,524 | 5,352,996 | |||||
| Lease liability—current | 110,551 | 190,471 | |||||
| Total current liabilities | 3,998,139 | 7,316,499 | |||||
| Lease liability—noncurrent | -- | -- | |||||
| Total liabilities | 3,998,139 | 7,316,499 | |||||
| Commitments and contingencies | |||||||
| Preferred stock, par value | 2,998,537 | -- | |||||
| Stockholders’ equity: | |||||||
| Common stock, par value | 52,237 | 21,859 | |||||
| Additional paid-in capital | 328,167,899 | 240,978,439 | |||||
| Accumulated other comprehensive loss | (10,240,645 | ) | (10,358,956 | ) | |||
| Accumulated deficit | (291,354,263 | ) | (181,134,378 | ) | |||
| Total stockholders’ equity | 26,625,228 | 49,506,964 | |||||
| Total liabilities and stockholders’ equity | $ | 33,621,904 | $ | 56,823,463 | |||
Aprea Therapeutics, Inc.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(Unaudited)
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||||
| 2022 | 2021 | 2022 | 2021 | |||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | $ | 1,117,576 | $ | 6,015,616 | $ | 15,870,867 | $ | 19,433,721 | ||||||||
| General and administrative | 3,082,618 | 3,414,795 | 18,849,549 | 10,183,953 | ||||||||||||
| Acquired in-process research and development | -- | -- | 76,020,184 | -- | ||||||||||||
| Total operating expenses | 4,200,194 | 9,430,411 | 110,740,600 | 29,617,674 | ||||||||||||
| Other income (expense): | ||||||||||||||||
| Interest income (expense) | 151,123 | (33 | ) | 205,585 | (1,678 | ) | ||||||||||
| Foreign currency (loss) gain | 24,353 | (21,907 | ) | 315,130 | 247,233 | |||||||||||
| Total other income (expense) | 175,476 | (21,940 | ) | 520,715 | 245,555 | |||||||||||
| Net loss | $ | (4,024,718 | ) | $ | (9,452,351 | ) | $ | (110,219,885 | ) | $ | (29,372,119 | ) | ||||
| Other comprehensive income (loss): | ||||||||||||||||
| Foreign currency translation | 26,161 | (207,608 | ) | 118,311 | (417,438 | ) | ||||||||||
| Total comprehensive loss | (3,998,557 | ) | (9,659,959 | ) | (110,101,574 | ) | (29,789,557 | ) | ||||||||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.12 | ) | $ | (0.45 | ) | $ | (4.17 | ) | $ | (1.39 | ) | ||||
| Weighted-average common shares outstanding, basic and diluted | 34,655,750 | 21,231,584 | 26,453,091 | 21,201,910 | ||||||||||||
FAQ
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