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Precision Oncology Through Synthetic Lethality September 2023 Forward-Looking Statements Certain information contained in this presentation includes “forward-looking statements”, within the meaning of Secti

Key Takeaway: Aprea Therapeutics has reported promising findings regarding its investigational ATR inhibitor, ATRN-119, which has demonstrated potential as a best-in-class treatment with a favorable toxicity profile compared to competitors. In a recent study, a dog undergoing treatment with ATRN-119 maintained normal levels of blood cells and experienced negligible changes in body weight. However, Aprea has cautioned that forward-looking statements regarding the product's development are subject to various risks, including the dependency on future financing and the inherent uncertainties of clinical trials.

Market Sentiment Analysis

POSITIVE FACTORS

  • ATRN-119 shows potential as a best-in-class ATR inhibitor with a differentiated profile.
  • Reduced toxicity of ATRN-119 could make it attractive for patients as a single agent.
  • Safety profile indicates normal blood cell levels and minimal body weight changes in studies.

CONCERNS & RISKS

  • Forward-looking statements indicate potential risks related to clinical trial outcomes.
  • Dependency on additional financing raises concerns about future operational capabilities.
  • Limited history with preclinical assets poses uncertainty for development.

Full Press Release Details

For the dog receiving ATRN-119, reduced levels of reticulocytes and neutrophils were noted with prolonged treatment but remained within normal ranges and body weight changes were negligible (-2% to +4%). ATRN-119: Potential Best-in-Class Oral ATR Inhibitor With Structurally Differentiated Core, Backbone, and Toxicity Profile ATRN-119 potential for reduced toxicity could make it a preferred ATR inhibitor as a single agent, as well as a candidate for combination with standard-of-care therapies. 2023 Aprea Therapeutics, Inc.
ATRN-119 - 20 mg/kg/day for 7 days, followed by 40 mg/kg/day for 7 days and finally 50 mg/kg/day for 7 days, all P.O. Competitor ATRi- administered at a clinically equivalent dose range during 21 days, P.O. By day 4 of dosing, the dog receiving the competitor ATRi exhibited severe reduction in multiple blood cell lineages including reticulocytes. Continued dosing of competitor ATRi for three weeks resulted in significant reduction of white blood cells, red blood cells and hemoglobin levels, and was accompanied by severe body weight loss (-15%).
(4) Repare announced a worldwide license and collaboration agreement with Roche on June 1, 2022 (5) Preliminary Phase 1 Data From Ongoing First-in-Human Phase 1/2 TRESR Study of RP-3500, AACR 2022 ATR Landscape Drives Potential Competitive Advantage for ATRN-119 Current ATRs Structurally Similar in Core, Backbone, and Toxicity Profile 2023 Aprea Therapeutics, Inc.
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 presentation. We undertake no obligation to update such forward-looking statements to reflect subsequent events or circumstances, except to the extent required by law or regulation. 2023 Aprea Therapeutics, Inc.
Securities and Exchange Commission, including our Annual Reports on Form 10-K and Quarterly Reports on Form 10-Q. Forward-looking statements regarding our product candidates are also subject to additional risks and uncertainties, including without limitation, with respect to: our dependence on additional financing to fund our operations and complete the development and commercialization of our product candidates, and the risks that raising such additional capital may restrict our operations or require us to relinquish rights to our technologies or product candidates; our limited history and preclinical status of the assets we acquired from Atrin Pharmaceuticals Inc.; our business plan or the likelihood of the successful implementation of such business plan; the timing of initiation of planned clinical trials for our product candidates; the future success of such trials; the successful implementation of our research and development programs and collaborations and the interpretation of the results and findings of such programs and collaborations and whether such results are sufficient to support the future success of our product candidates; the success, timing and cost of our anticipated clinical trials for our current product candidates; the timing of initiation, futility analyses, data presentation, reporting and publication and receipt of interim results (including, without limitation, any preclinical results or data); any statements about our understanding of product candidates mechanisms of action and interpretation of preclinical and early clinical results from its clinical development programs and any collaboration studies; and other factors, including legislative, regulatory, political and economic developments not within our control.
Any or all of the forward-looking statements may turn out to be wrong or be affected by inaccurate assumptions our management team 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 and timing of our clinical trials or other studies and the other risks set forth in our filings with the U.S.
We may, in some cases use terms such as predicts, believes, potential, continue, anticipates, estimates, expects, plans, intends, may, could, might, likely, will, should or other words that convey uncertainty of the future events or outcomes to identify these forward-looking statements. The forward-looking statements are based on current beliefs and expectations of our management team that involve risks, potential changes in circumstances, assumptions, and uncertainties.

Frequently Asked Questions

What effects were observed in dogs treated with ATRN-119?

Dogs receiving ATRN-119 showed reduced reticulocyte and neutrophil levels, but they remained normal and overall body weight changes were minimal.

How does ATRN-119 compare to competitor ATR inhibitors?

ATRN-119 demonstrated lower toxicity compared to a competitor ATR inhibitor, which caused significant blood cell reduction and severe weight loss.

What dosing schedule was used for ATRN-119?

The dosing schedule for ATRN-119 included 20 mg/kg/day for 7 days, 40 mg/kg/day for 7 days, and 50 mg/kg/day for 7 days.

Are there risks associated with forward-looking statements?

Yes, forward-looking statements carry risks and uncertainties that may affect actual results, including clinical trials and financial needs.

What is the significance of ATRN-119's toxicity profile?

ATRN-119's potentially reduced toxicity may make it a preferred choice for monotherapy and in combination with standard treatments.

Last updated: Sep 11, 2023