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Aprea Therapeutics: early WEE1 data show dose-dependent efficacy and favorable safety profile
Aprea Therapeutics presented early clinical data at the H.C. Wainwright conference on its oral WEE1 inhibitor showing dose-dependent responses, including a first partial response at 150 mg and a confirmed partial response at 220 mg. The safety profile was described as unusually favorable for heavily pretreated patients, which could facilitate combination studies. Funding of $41 million is expected to secure the cash runway into the first quarter of 2028; the company is concentrating investments on the WEE1 program and seeking a partner for the ATR inhibitor. Additional data, including results from the 300 mg cohort, are expected in the coming quarters. » More on de.investing.com
Aprea Therapeutics reports patent portfolio of 58 patents and applications
Aprea Therapeutics announces an intellectual property portfolio of 28 granted patents and 30 pending applications. The WEE1 program, including the lead candidate APR-1051 (Phase-1 study ACESOT-1051), is covered by multiple US and non‑US filings; potential exclusivity could extend to 2047. The ATR program has issued US and non‑US patents and pending applications that, if granted, could provide protection through 2045. Aprea has deprioritized development of ATRN-119 as monotherapy in favor of APR-1051 and will instead evaluate ATRN-119 in combination therapies. » More on de.investing.com
Aprea Therapeutics to present data update on APR-1051 phase‑1 study in Q4 2026
Aprea Therapeutics will present data from the ongoing phase‑1 study ACESOT‑1051 of APR‑1051 at a scientific conference in Q4 2026. Dose escalation is currently in the 300 mg cohort (10–500 mg planned), and the number of active sites has been increased from three to ten, which is expected to raise the recruitment rate to six to ten patients per month by Q4 2026. The program will be expanded to include combinations with standard therapies in HPV‑positive head-and-neck squamous cell carcinoma and colorectal cancer; recruitment will also be expanded to at least 50 patients with serous endometrial carcinoma or cyclin‑E–overexpressing, platinum‑resistant ovarian cancer. Completion of dose escalation and the backfill expansion is expected in Q2 2027. » More on de.investing.com
Financials
| (EUR) | June 2026 | |
|---|---|---|
| Revenue | 0 | 100.00% |
| Gross profit | 0 | 100.00% |
| Net profit | -3.15m | 14.51% |
| EBITDA | -3.14m | 14.52% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €7.89m |
Number of shares | 12.38m |
52-week high/low | €1.47 - €0.48 |
| Dividends | No |
Beta | 1.63 |
P/E ratio | -0.57 |
PEG ratio | -0.01 |
P/B ratio | 1.02 |
P/S ratio | 0.00 |
Company profile
Aprea Therapeutics, Inc. ist ein biopharmazeutisches Unternehmen im klinischen Stadium, das sich auf die Entwicklung und Vermarktung neuartiger Krebstherapeutika konzentriert, die auf DNA-Schadensreaktionswege abzielen. Der führende Produktkandidat ist ATRN-119, ein oral zu verabreichender ATR-Inhibitor, der sich in einer klinischen Studie der Phase 1/2a zur Behandlung von Patienten mit fortgeschrittenen soliden Tumoren befindet. Die Produktpipeline des Unternehmens umfasst außerdem ATRN-Backup, einen ATR-Inhibitor, ATRN-W1051 zur Behandlung von Antitumoraktivitäten und ATRN-DDRi. Aprea Therapeutics, Inc. hat seinen Sitz in Boston, Massachusetts.
| Name | Aprea Therapeutics |
| CEO | Oren Gilad |
| Headquarters | Boston,
pa USA |
| Website | |
| Sector | Materials |
| Industry | Chemicals |
| IPO | 03/10/2019 |
| Employees | 8 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | APRE |