| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 488.24K | 1.50M | 583.23K | 0.00 | 0.00 | 0.00 |
| Gross Profit | -6.27M | -7.86M | 576.18K | -16.40M | -271.68K | -229.61K |
| EBITDA | -13.65M | -14.30M | -14.28M | -37.37M | -36.86M | -53.25M |
| Net Income | -13.04M | -12.96M | -14.29M | -112.66M | -36.54M | -53.92M |
Balance Sheet | ||||||
| Total Assets | 14.32M | 23.98M | 22.65M | 30.16M | 56.82M | 92.81M |
| Cash, Cash Equivalents and Short-Term Investments | 13.72M | 22.85M | 21.61M | 28.79M | 53.08M | 89.02M |
| Total Debt | 0.00 | 0.00 | 0.00 | 0.00 | 190.47K | 335.16K |
| Total Liabilities | 2.68M | 4.67M | 4.39M | 4.51M | 7.32M | 15.41M |
| Stockholders Equity | 11.64M | 19.31M | 18.26M | 25.64M | 49.51M | 77.40M |
Cash Flow | ||||||
| Free Cash Flow | -13.54M | -13.57M | -12.27M | -25.01M | -37.69M | -41.83M |
| Operating Cash Flow | -13.54M | -13.56M | -12.18M | -25.01M | -37.69M | -41.80M |
| Investing Cash Flow | 0.00 | -15.48K | -93.09K | 0.00 | 0.00 | -25.71K |
| Financing Cash Flow | 945.82K | 14.82M | 5.14M | 682.97K | 1.75M | 150.95K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
52 Neutral | $6.63M | -0.02 | -655.85% | ― | ― | -228.89% | |
52 Neutral | $10.24M | -0.33 | -189.72% | ― | ― | 70.57% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $18.86M | -0.72 | -70.67% | ― | 6.29% | 7.42% | |
46 Neutral | $13.86M | -0.02 | -179.40% | ― | ― | 94.52% | |
43 Neutral | $6.29M | -0.42 | -74.72% | ― | -62.75% | 23.87% |
On January 9, 2026, Aprea Therapeutics updated its corporate presentation, outlining a development roadmap through 2026 that highlights multiple DDR-focused drug candidates and clinical milestones in early-stage oncology trials. The company detailed progress on its ATR inhibitor ATRN-119, for which further monotherapy enrollment has been paused in favor of exploring combination strategies, and on its WEE1 inhibitor APR-1051, which is being advanced toward clinical proof-of-concept as a potentially safer alternative in a target class historically limited by toxicity. The refreshed deck emphasizes Aprea’s strategy to capitalize on synthetic lethality as a validated cancer-killing approach, positioning the firm to benefit from rising global cancer incidence and sustained demand for targeted therapies, while showcasing an experienced management team and board with deep expertise in oncology drug development and commercialization.
The most recent analyst rating on (APRE) stock is a Hold with a $0.89 price target. To see the full list of analyst forecasts on Aprea Therapeutics stock, see the APRE Stock Forecast page.
On December 8, 2025, Aprea Therapeutics entered into a securities purchase agreement with accredited investors and company insiders to issue and sell 2,623,023 shares of common stock and warrants in a private placement, expected to close on December 10, 2025, for approximately $3.1 million. This financing is anticipated to extend Aprea’s cash runway into Q1 2027, supporting its clinical programs and general corporate purposes, with Maxim Group LLC acting as the sole placement agent.
The most recent analyst rating on (APRE) stock is a Buy with a $10.00 price target. To see the full list of analyst forecasts on Aprea Therapeutics stock, see the APRE Stock Forecast page.
On November 12, 2025, Aprea Therapeutics reported its third-quarter financial results and provided updates on its clinical programs. The company highlighted progress in its WEE1 and ATR inhibitor programs, with APR-1051 showing promising results in a Phase 1 trial and ATRN-119 reaching a recommended Phase 2 dose. Aprea’s financials showed a reduction in operating loss and R&D expenses compared to the previous year, with cash reserves expected to support operations into late 2026.
The most recent analyst rating on (APRE) stock is a Buy with a $10.00 price target. To see the full list of analyst forecasts on Aprea Therapeutics stock, see the APRE Stock Forecast page.
On October 24, 2025, Aprea Therapeutics announced promising early results from their ACESOT-1051 trial for the WEE1 Kinase Inhibitor APR-1051, showing that 3 out of 4 patients achieved stable disease at a 100 mg dose level. The trial, which focuses on heavily pretreated patients with gastrointestinal and gynecologic malignancies, observed disease stabilization in tumors with specific mutations, supporting the mechanistic rationale for APR-1051’s development. The company is encouraged by these findings and is progressing to a higher dose level in the ongoing study.
The most recent analyst rating on (APRE) stock is a Buy with a $10.00 price target. To see the full list of analyst forecasts on Aprea Therapeutics stock, see the APRE Stock Forecast page.
On October 15, 2025, Aprea Therapeutics announced the recommended Phase 2 dose of 1,100 mg once daily for ATRN-119 in its ongoing ABOYA-119 study for advanced solid tumors. The company is pausing further monotherapy enrollment to focus on combination therapies, leveraging ATRN-119’s potential synergistic effects with DNA-damaging agents. This strategic shift aims to enhance the therapeutic potential of ATRN-119, with ongoing discussions for combination studies in HPV+ head and neck cancer and other indications.
The most recent analyst rating on (APRE) stock is a Buy with a $10.00 price target. To see the full list of analyst forecasts on Aprea Therapeutics stock, see the APRE Stock Forecast page.