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    Predictive Oncology Issues Shareholder Letter: Well Financed to Support Expanded U.S. Availability and E.U. Launch of ChemoFx® and Pursuit of Other High-Value AI-Driven Drug Discovery and Development Opportunities

    7/15/25 9:00:00 AM ET
    $POAI
    Industrial Specialties
    Health Care
    Get the next $POAI alert in real time by email

    $10 million securities purchase agreement provides efficient and flexible funding in support of strategic multi-million dollar growth initiatives

    Discussions underway to expand adoption of ChemoFx in the U.S. and accelerate initial launch in Europe

    PITTSBURGH, July 15, 2025 (GLOBE NEWSWIRE) -- Predictive Oncology Inc. (NASDAQ:POAI), a leader in AI-driven drug discovery, today issued the following shareholder update:

    To my fellow Shareholders,

    The past several weeks have been particularly noteworthy and productive at Predictive Oncology, and I wanted to take this opportunity to provide a brief recap of recent developments.

    Preparing for aggressive market expansion of ChemoFx® in the U.S. and de novo Launch in Europe

    I'd like to begin with ChemoFx, which is our proprietary live-cell tumor profiling assay that uses a patient's own cells to measure chemotherapy responses in vitro, providing personalized guidance for treatment selection. By testing multiple chemotherapies on a patients' cancer cells before treatment selection, ChemoFx helps determine which chemotherapies are more likely to be effective on the tumor and which are less likely to provide benefit to the patient. With these data in-hand, oncologists can make better and faster treatment decisions – eliminating the current "trial-and-error" approach – which could go a long way towards improving patient outcomes while saving precious time and money.

    This flagship assay, which stands as a renewable and extensible asset for the Company, was the primary assay by which the Company acquired more than 150,000 tumor samples, analyzed more than twenty-five years of drug response data and represents a significant opportunity for the Company to steadily augment the biobank, consistently develop novel drug response data and increase the likelihood of recurring revenue. The groundwork to expand availability of ChemoFx in the U.S is already underway, including meaningful and productive discussions with potential channel partners, and other end-users, including R&D-based pharmaceutical manufacturers.

    As we look to develop the next generation of ChemoFx, the Company anticipates the ability to extend beyond gynecological cancers, into other tumor types, including breast, colon and lung.

    More importantly, the ability to obtain a patient tumor sample and monitor its growth and drug response as it transitions from a 2D cell culture to cryopreservation and then to 3D cell spheroids exemplifies the relevance and availability of our samples for high-throughput drug discovery, personalized medicine, and biomarker discovery. The utilization of cryopreserved dissociated tumor cells (DTCs) represents a scalable resource for research and clinical trials with viable primary tumor material.

    The high throughput screening [HTS] market is projected to reach $69.5 billion by 2032, reflecting a CAGR of 12.18%, according to SNS Insider research. There is a growing adoption of 3D cell cultures which provide more physiologically relevant models for screening, enhancing the predictive power of HTS assays.

    Collectively, these capabilities directly support the Company's AI-driven drug discovery initiatives by generating high-quality data that feeds into predictive models and supports biomarker discovery, companion diagnostics, and clinical trial design.

    Core AI-Driven Drug Discovery, Biomarker Discovery and Drug Repurposing Initiatives Continue to Advance

    In parallel with our ChemoFx commercialization activities, we remain focused on our drug and biomarker discovery and drug repurposing initiatives that we will advance either independently or in collaboration with strategic partners.

    Our ability to integrate patient and tumor heterogeneity into the earliest phases of drug and biomarker discovery, driven by our biobank of 150,000 tumor samples across 137 cancer types, makes us truly unique in an industry that is growing and evolving rapidly.

    We previously talked about our successful work with UPMC Magee-Womens Hospital, where we successfully developed AI-powered multi-omic machine learning models that predict short- and long-term survival outcomes in ovarian cancer patients—outperforming models based solely on clinical data.

    Building on the success of the Magee study, we identified novel ovarian cancer biomarkers linked to patient survival and drug response using advanced deep learning methods. Models like this have applications well beyond drug and biomarker discovery and can also be integrated into day-to-day clinical practice, helping guide treatment decisions and potentially improving patient management and outcomes.

    Regarding drug repurposing, we previously talked about our success screening a curated set of such compounds using active machine learning that led to the identification of three candidates worth re-evaluating in ovarian and colon cancer. We are building on this success by applying this approach to a broader range of publicly available compounds. The ability to transition a shelved drug candidate back into clinical development is of enormous value to the biopharmaceutical industry, and I believe we are at the forefront of this initiative.

    Securities Purchase Agreement Provides an Efficient and Flexible Source of Funding

    To efficiently and effectively execute on the US expansion and EU launch of ChemoFx, and simultaneously pursue the emerging opportunities utilizing our core AI and machine learning capabilities, we were very pleased to have recently announced a $10 million Securities Purchase Agreement (SPA) with Yorkville Advisors Global, LP. This agreement, which was executed at terms that we believe are attractive to our company, provides us with the right, but not the obligation, to opportunistically sell POAI shares to Yorkville when market conditions are deemed to be favorable. Notably, there are no warrants or other financial derivatives associated with the SPA.

    We regard this agreement with Yorkville as a true partnership that we think will be mutually beneficial, and we are grateful to them for their support of our company and our vision.

    In closing, we continue to methodically take steps to create a solid foundation from which to drive meaningful and sustained growth in 2026 and beyond. I would like to once again thank you, our shareholders, for your continued support. I believe we are uniquely positioned to lead the next wave of advancement in precision oncology, and I am very optimistic about what the future holds for our industry and our company.

    Sincerely,

    Raymond

    Raymond Vennare

    Chief Executive Officer and Chairman of the Board, Predictive Oncology

    About Predictive Oncology

    Predictive Oncology is on the cutting edge of the rapidly growing use of artificial intelligence and machine learning to expedite early drug discovery and enable drug development for the benefit of cancer patients worldwide. The company's scientifically validated AI platform, PEDAL, is able to predict with 92% accuracy if a tumor sample will respond to a certain drug compound, allowing for a more informed selection of drug/tumor type combinations for subsequent in-vitro testing. Together with the company's vast biobank of more than 150,000 assay-capable heterogenous human tumor samples, Predictive Oncology offers its academic and industry partners one of the industry's broadest AI-based drug discovery solutions, further complimented by its wholly owned CLIA laboratory facility. Predictive Oncology is headquartered in Pittsburgh, PA.

    Investor Relations Contact:

    Mike Moyer

    LifeSci Advisors, LLC

    [email protected]

    Forward-Looking Statements

    Certain statements made in this press release are "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These forward- looking statements reflect Predictive Oncology's current expectations and projections about future events and are subject to substantial risks, uncertainties and assumptions about Predictive Oncology's operations and the investments Predictive Oncology makes. All statements, other than statements of historical facts, included in this press release regarding our strategy, future operations, future financial position, future revenue and financial performance, projected costs, prospects, changes in management, plans and objectives of management are forward-looking statements. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "plan," "would," "target" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Predictive Oncology's actual future performance may materially differ from that contemplated by the forward-looking statements as a result of a variety of factors including, among other things, factors discussed under the heading "Risk Factors" in Predictive Oncology's filings with the SEC. Except as expressly required by law, Predictive Oncology disclaims any intent or obligation to update these forward-looking statements. Predictive Oncology does not give any assurance that Predictive Oncology will achieve its expectations described in this press release.



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