Recent Updates
Recently added Catalysts
APRE Positive Sentiment Score: 75/100

Aprea Therapeutics Reports Second Quarter 2024 Financial Results and Provides Business Update Enrollment commenced in the ACESOT-1051 Phase 1 trial evaluating APR-1051 - no myelosuppression observed in the first of eight

Key Takeaway: Aprea Therapeutics announced its financial results for Q2 2024, highlighting the initiation of the ACESOT-1051 Phase 1 trial for APR-1051, a WEE1 kinase inhibitor. The trial has begun enrolling patients, with no observed myelosuppression in the initial group. The company reported $28.7 million in cash, extending its financial runway into Q4 2025. However, Aprea also noted a net loss of $3.47 million for the quarter, raising some concerns regarding its long-term financial viability.

Market Sentiment Analysis

POSITIVE FACTORS

  • Enrollment in the ACESOT-1051 Phase 1 trial has commenced.
  • No myelosuppression has been observed in the first cohort of patients.
  • Aprea has a strong cash position with $28.7 million available, extending their runway into Q4 2025.
  • The company's CEO expresses confidence in the potential of APR-1051 as a best-in-class treatment.

CONCERNS & RISKS

  • The company reported a net loss of $3.47 million for the second quarter.
  • Operating expenses have increased compared to the previous year, raising concerns about long-term financial sustainability.
  • The report includes forward-looking statements, indicating uncertainty in clinical trial outcomes.

Full Press Release Details

Aprea Therapeutics Reports Second Quarter 2024 Financial Results and Provides Business Update
Enrollment commenced in the ACESOT-1051 Phase 1 trial evaluating APR-1051 - no myelosuppression observed in the first of eight planned cohorts at sub-therapeutic dose
$28.7 million in cash and cash equivalents as of June 30, 2024 with cash runway extended into Q4 2025
DOYLESTOWN, PA, August 12, 2024 (GLOBE NEWSWIRE) - Aprea Therapeutics, Inc. (Nasdaq: APRE) ("Aprea", or the "Company"), a clinical-stage biopharmaceutical company focused on precision oncology through synthetic lethality, today reported financial results for the second quarter ended June 30, 2024, and provided a business update.
"Aprea continues to make excellent progress advancing its clinical pipeline of therapeutic candidates," said Oren Gilad, Ph.D., President and Chief Executive Officer of Aprea. "We initiated enrollment in the ACESOT-1051 trial, advancing a second clinical asset in our pipeline, APR-1051. APR-1051 is a next-generation inhibitor of WEE1 kinase which has been designed to limit toxicity. Based on its unique characteristics, we believe it could be best in class. We continue to enroll patients in the ABOYA-119 trial evaluating ATRN-119, our ATR inhibitor. We believe that our ongoing progress positions Aprea at the forefront of synthetic lethality drug development. We remain committed to developing new treatments that have a positive impact on the lives of cancer patients while creating value for our shareholders."
Key Business Updates and Potential Upcoming Key Milestones
ACESOT-1051: A Biomarkers Focused, Phase 1 Trial of Oral WEE1 inhibitor, APR-1051, initiated
ABOYA-119: Ongoing Clinical Trial Evaluating ATR inhibitor, ATRN-119
Select Financial Results for the Second Quarter ended June 30, 2024
Aprea Therapeutics, Inc. is a clinical-stage biopharmaceutical company headquartered in Doylestown, Pennsylvania, focused on precision oncology through synthetic lethality. The Company's lead program is ATRN-119, a clinical-stage small molecule ATR inhibitor in development for solid tumor indications. APR-1051, an oral, small-molecule WEE1 inhibitor, recently entered the clinic. 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 and on information currently available to management that involve risks, potential changes in circumstances, assumptions, and uncertainties. All statements contained in this press release other than statements of historical fact are forward-looking statements, including statements regarding our ability to develop, commercialize, and achieve market acceptance of our current and planned products and services, our research and development efforts, including timing considerations and other matters regarding our business strategies, use of capital, results of operations and financial position, and plans and objectives for future operations. 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, without limitation, risks related to the success, timing, and cost of our ongoing clinical trials and anticipated clinical trials for our current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including our ability to fully fund our disclosed clinical trials, which assumes no material changes to our currently projected expenses), futility analyses, presentations at conferences and data reported in an abstract, and receipt of interim or preliminary results (including, without limitation, any preclinical results or data), which are not necessarily indicative of the final results of our ongoing clinical trials, our understanding of product candidates mechanisms of action and interpretation of preclinical and early clinical results from its clinical development programs, and the other risks, uncertainties, and other factors described under "Risk Factors," "Management's Discussion and Analysis of Financial Condition and Results of Operations" and elsewhere in the documents we file 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 update such forward-looking statements for any reason, except as required by law.
Ignacio Guerrero-Ros, Ph.D., or David Schull
Aprea Therapeutics, Inc.
Consolidated Balance Sheets
June 30, December 31,
2024 2023
Assets
Current assets:
Cash and cash equivalents $ 28,694,694 $ 21,606,820
Prepaid expenses and other current assets 865,092 914,275
Total current assets 29,559,786 22,521,095
Property and equipment, net 92,379 88,362
Restricted cash 41,260 40,717
Other noncurrent assets 271,162 -
Total assets $ 29,964,587 $ 22,650,174
Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable $ 964,327 $ 1,670,369
Accrued expenses 2,079,163 2,186,262
Deferred revenue 50,739 528,974
Total current liabilities 3,094,229 4,385,605
Total liabilities 3,094,229 4,385,605
Commitments and contingencies
Series A convertible preferred stock, $0.001 par value, 40,000,000 shares authorized; 56,227 shares issued and outstanding at June 30, 2024 and December 31, 2023, respectively. 1,311,063 1,311,063
Stockholders' equity:
Common stock, $0.001 par value, 400,000,000 shares authorized, 5,430,215 and 3,736,673 shares issued and outstanding at June 30, 2024 and December 31, 2023, respectively. 5,430 3,736
Additional paid-in capital 350,566,533 335,644,204
Accumulated other comprehensive loss (10,649,364) (10,611,273)
Accumulated deficit (314,363,304) (308,083,161)
Total stockholders' equity 25,559,295 16,953,506
Total liabilities and stockholders' equity $ 29,964,587 $ 22,650,174
Aprea Therapeutics, Inc.
Consolidated Statements of Operations and Comprehensive Loss
Three Months Ended June 30, Six Months Ended June 30,
2024 2023 2024 2023
(Unaudited)
Grant revenue $ 561,574 $ 249,688 $ 942,143 $ 249,688
Operating expenses:
Research and development 2,557,679 2,202,657 4,158,052 3,459,199
General and administrative 1,850,819 1,698,712 3,780,685 5,064,673
Total operating expenses 4,408,498 3,901,369 7,938,737 8,523,872
Loss from operations (3,846,924) (3,651,681) (6,996,594) (8,274,184)
Other income (expense):
Interest income, net 382,374 336,221 665,777 592,631
Foreign currency gain (loss) (5,502) 56,363 50,674 42,566
Total other income 376,872 392,584 716,451 635,197
Net loss $ (3,470,052) $ (3,259,097) $ (6,280,143) $ (7,638,987)
Other comprehensive (loss) gain:
Foreign currency translation (23,008) (73,420) (38,091) (11,464)
Total comprehensive loss (3,493,060) (3,332,517) (6,318,234) (7,650,451)
Net loss per share attributable to common stockholders, basic and diluted $ (0.58) $ (0.87) $ (1.24) $ (2.18)
Weighted-average common shares outstanding, basic and diluted 5,937,291 3,731,571 5,067,809 3,497,329

Frequently Asked Questions

What is the ACESOT-1051 trial about?

The ACESOT-1051 trial is a Phase 1 study evaluating the oral WEE1 inhibitor APR-1051.

What financial position did Aprea Therapeutics report for Q2 2024?

Aprea reported $28.7 million in cash and equivalents, extending its runway to Q4 2025.

What is APR-1051 designed to do?

APR-1051 is designed as a next-generation WEE1 kinase inhibitor to limit toxicity.

How is Aprea dedicated to cancer treatment?

Aprea is committed to developing treatments that positively impact cancer patients' lives.

What are Aprea's ongoing clinical trials?

Aprea is enrolling patients in ACESOT-1051 for APR-1051 and ABOYA-119 for ATRN-119.

Last updated: Aug 12, 2024