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Aprea Therapeutics (NASDAQ: APRE) closes $30M oversubscribed funding

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Aprea Therapeutics, Inc. closed an oversubscribed private placement, raising total gross proceeds of approximately $30 million. The funding comes from a group led by Soleus Capital, with new and existing investors and certain insiders participating.

The company issued pre-funded warrants to purchase up to about 37.2 million shares of common stock and additional warrants to purchase up to about 37.2 million shares. Warrant exercise prices range around $0.808 and $0.683 per share. Aprea plans to use net proceeds for general corporate purposes and to advance development of its lead WEE1 inhibitor APR-1051, including expanding its ACESOT-1051 study into selected biomarker-defined tumor populations.

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Insights

$30M private placement strengthens Aprea’s cash for APR-1051 development.

Aprea Therapeutics completed an oversubscribed private placement for gross proceeds of about $30 million, issuing pre-funded warrants and standard warrants covering up to roughly 74.4 million common shares in total. The structure concentrates near-term cash inflow while deferring potential share issuance to warrant exercise.

Management states the net proceeds will support general corporate purposes and research and development, particularly the ongoing ACESOT-1051 study of WEE1 inhibitor APR-1051. Plans include enrolling at least 50 patients with uterine serous carcinoma and cyclin E-overexpressing, platinum-resistant ovarian cancer, aiming to refine the clinical path in biomarker-selected populations.

The warrants are immediately exercisable at $0.683 per share and expire on December 31, 2029, or may be forfeited 30 days after exercise of pre-funded warrants, which could limit overhang duration depending on holder behavior. Actual dilution and capital realized will depend on future warrant exercises under market conditions.

Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Private placement gross proceeds $30 million Total gross proceeds from oversubscribed private placement
Pre-funded warrants issued ≈37.2 million shares Pre-funded warrants to purchase common stock in the offering
Additional warrants issued ≈37.2 million shares Standard warrants to purchase common stock in the offering
Pre-funded warrant purchase price $0.808 minus $0.001 Per pre-funded warrant purchase price structure
Warrant exercise price $0.683 per share Exercise price for common stock warrants
Warrant expiry date December 31, 2029 Expiration for standard warrants, subject to forfeiture terms
Planned patient enrollment At least 50 patients ACESOT-1051 study in USC and PROC populations
pre-funded warrants financial
"the Company sold (i) pre-funded warrants to purchase up to an aggregate of approximately 37.2 million shares"
Pre-funded warrants are financial instruments that give investors the right to purchase a company's stock at a set price, but with most or all of the purchase price paid upfront. They function like a coupon or gift card for stock, allowing investors to buy shares later at a fixed price, which can be beneficial if they want to avoid future price increases. This makes them important for investors seeking flexibility and certainty in their investment plans.
WEE1 mechanism technical
"expansion into selected patient populations where WEE1 mechanism is well suited"
platinum-resistant ovarian cancer medical
"cyclin E-overexpressing, platinum-resistant ovarian cancer (PROC)"
A form of ovarian cancer that stops responding to standard platinum-based chemotherapy, typically when the disease returns within about six months after treatment; think of it like a pest becoming resistant to a once-effective pesticide. It matters to investors because this resistance creates a large unmet medical need, shaping demand for new drugs, clinical trial strategies, regulatory priority and potential pricing — all of which can materially affect company value and market opportunity.
Regulation D regulatory
"under Section 4(a)(2) of the Securities Act of 1933, as amended (the “Securities Act”), and Regulation D promulgated thereunder"
Regulation D is a set of rules that govern how companies can raise money from investors without going through the full process required for public stock offerings. It provides simplified options for private placements, making it easier for companies to seek investments from a smaller group of investors. For investors, it offers opportunities to invest in private companies, often with fewer restrictions, but also with different levels of risk and disclosure.
Section 4(a)(2) of the Securities Act regulatory
"made in a private placement under Section 4(a)(2) of the Securities Act of 1933"
A legal exemption that allows a company to sell securities directly to a limited group of buyers without registering the offering with the Securities and Exchange Commission. Think of it like a private sale among known parties rather than a public auction: it can speed fundraising and reduce disclosure requirements, but it also means less public information, lower liquidity and resale restrictions—factors investors should consider when weighing risk and exit options.
biomarker-defined cancers medical
"targeted therapies for patients with biomarker-defined cancers"
0001781983false00017819832026-04-012026-04-01

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d)

of the Securities Exchange Act of 1934

April 1, 2026

Date of Report (Date of earliest event reported)

Aprea Therapeutics, Inc.

(Exact name of registrant as specified in its charter)

Delaware

001-39069

84-2246769

(State or other jurisdiction
of incorporation)

(Commission
File Number)

(IRS Employer
Identification No.)

    

3805 Old Easton Road
Doylestown, PA
(Address of principal executive offices)

18902
(Zip Code)

Registrant’s telephone number, including area code: (215) 948-4119

(Former name or former address, if changed since last report): Not applicable

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

  ​ ​

Trading Symbol(s)

  ​ ​

Name of each exchange on
which registered

Common stock, par value $0.001 per share

APRE

The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

Item 7.01 Regulation FD Disclosure.

On April 1, 2026, Aprea Therapeutics, Inc. issued a press release regarding the closing of its previously announced private placement for gross proceeds of approximately $30 million.  The press release is attached hereto as Exhibit 99.1 and is incorporated herein in its entirety by reference.

The information furnished under this Item 7.01, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, and shall not be deemed incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.

Item 9.01Financial Statements and Exhibits.

(d) Exhibits.

Exhibit
Number

  ​ ​ ​

Description

99.1

Press Release of Aprea Therapeutics, Inc., dated as of April 1, 2026

104

Cover Page Interactive Data File (embedded within the inline XBRL document).

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Aprea Therapeutics, Inc.

Dated: April 1, 2026

By:

/s/ Oren Gilad

Name:

Oren Gilad, Ph.D.

Title:

President and Chief Executive Officer

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Exhibit 99.1

Aprea Therapeutics Announces Closing of Oversubscribed $30 Million Private Placement

Funding will support ongoing development of APR-1051, including expansion into selected patient populations where WEE1 mechanism is well suited

DOYLESTOWN, PA, April 1, 2026 (GLOBE NEWSWIRE) — Aprea Therapeutics, Inc. (Nasdaq: APRE) (“Aprea”, or the “Company”), a clinical-stage precision medicine oncology company focused on the discovery and development of targeted therapies for patients with biomarker-defined cancers, today announced the closing of its previously announced oversubscribed private placement financing. Total gross proceeds from the offering are approximately $30 million to the Company before deducting placement agent fees and other private placement expenses (the “Offering”).  The Offering closed on March 31, 2026.  The Company intends to use the upfront net proceeds for general corporate purposes and for research and development expenses.  

The private placement was led by Soleus Capital with participation from other new investors, including Vestal Point Capital and Squadron Capital Management, existing investors and certain insiders of the Company.

In connection with the Offering the Company sold (i) pre-funded warrants to purchase up to an aggregate of approximately 37.2 million shares of common stock (“Pre-Funded Warrants”), for a purchase price equal to $0.808, minus $0.001 per Pre-Funded Warrant, and (ii) warrants to purchase up to an aggregate of approximately 37.2 million shares of common stock. The warrants have an exercise price of $0.683 per share, are exercisable immediately upon issuance, and expire on December 31, 2029, or will be forfeited 30 calendar days after a holder exercises their Pre-Funded Warrants, proportional to the amount so exercised.

“This transformational financing is a significant commitment by top-tier biotech investors who believe in the potential of APR1-1051 to impact the lives of cancer patients,” said Oren Gilad, Ph.D., President and CEO of Aprea. “We believe the proceeds will accelerate the advancement of the ongoing ACESOT-1051 study.  Our immediate goal is to expand evaluation of APR-1051 in biologically selected tumor populations where we believe WEE1 inhibition may have meaningful therapeutic relevance. We plan to enroll at least 50 patients with uterine serous carcinoma (USC) and cyclin E-overexpressing, platinum-resistant ovarian cancer (PROC). We believe this strategy will sharpen the clinical development path for APR-1051 and accelerate insight generation in biomarker-defined patient populations most likely to benefit from WEE1 inhibition.”

Oppenheimer & Co. Inc. acted as the lead placement agent for the private placement. Maxim Group LLC acted as co-lead placement agent for the private placement.


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The offer and sale of the foregoing securities were made in a private placement under Section 4(a)(2) of the Securities Act of 1933, as amended (the “Securities Act”), and Regulation D promulgated thereunder, and the securities have not been registered under the Securities Act or applicable state securities laws. Accordingly, the securities may not be reoffered or resold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements of the Securities Act and such applicable state securities laws. The Company has agreed to file a registration statement with the Securities and Exchange Commission registering the resale of the securities purchased in the private placement.

This press release does not constitute an offer to sell or the solicitation of an offer to buy the securities, nor shall there be any sale of the securities in any state in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of such state. Any offering of the securities under the resale registration statement will only be made by means of a prospectus.

About Aprea

Aprea is a clinical-stage precision medicine oncology company focused on the discovery and development of targeted therapies for patients with biomarker-defined cancers. The Company is pioneering a new approach to treat cancer by exploiting vulnerabilities associated with cancer cell mutations. This approach was developed to kill tumors while minimizing the effect on normal, healthy cells. Aprea’s technology has potential applications across multiple cancer types, enabling it to target a range of tumors, including ovarian, endometrial, colorectal and head and neck squamous cell carcinoma. The company’s lead programs are APR-1051, an oral, small-molecule inhibitor of WEE1 kinase, and ATRN-119, a small molecule ATR inhibitor, both in clinical development for solid tumor indications. 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


Graphic

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, the failure to realize the anticipated benefits of the private placement and related transactions, market and other conditions, as well as 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.

Investor Contact:

Mike Moyer
LifeSci Advisors
mmoyer@lifesciadvisors.com


FAQ

What did Aprea Therapeutics (APRE) announce in its latest 8-K filing?

Aprea Therapeutics announced the closing of an oversubscribed private placement, raising approximately $30 million in gross proceeds. The financing involves pre-funded warrants and standard warrants and is intended to support general corporate purposes and research and development, including further clinical work on its WEE1 inhibitor APR-1051.

How much capital did Aprea Therapeutics (APRE) raise in the private placement?

Aprea Therapeutics raised total gross proceeds of about $30 million through an oversubscribed private placement. This capital infusion provides additional funding for the company’s operations, including advancing its oncology pipeline and supporting ongoing and planned clinical studies, particularly the ACESOT-1051 trial of WEE1 inhibitor APR-1051.

What securities did Aprea Therapeutics (APRE) issue in the $30M financing?

In the private placement, Aprea issued pre-funded warrants to purchase up to approximately 37.2 million common shares and additional warrants for up to approximately 37.2 million shares. The warrants are immediately exercisable at $0.683 per share and generally expire on December 31, 2029, subject to specified forfeiture conditions.

How will Aprea Therapeutics (APRE) use the proceeds from the private placement?

Aprea intends to use the upfront net proceeds from the $30 million private placement for general corporate purposes and research and development expenses. This includes accelerating development of APR-1051 and expanding the ACESOT-1051 study into biomarker-defined tumor populations such as uterine serous carcinoma and platinum-resistant ovarian cancer.

What clinical plans did Aprea Therapeutics (APRE) outline for APR-1051?

Aprea plans to use proceeds to advance APR-1051, its oral WEE1 kinase inhibitor, within the ACESOT-1051 study. The company expects to enroll at least 50 patients with uterine serous carcinoma and cyclin E-overexpressing, platinum-resistant ovarian cancer, focusing on biomarker-defined populations where WEE1 inhibition may be therapeutically relevant.

Filing Exhibits & Attachments

5 documents
Aprea Therapeutics, Inc.

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Biotechnology
Pharmaceutical Preparations
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United States
DOYLESTOWN