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Onco-Innovations' Inka Health Completes Analytical Work for AstraZeneca Canada, Advancing Pharmaceutical Analytics and Leading to Key Studies at ISPOR 2025

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VANCOUVER, BC / ACCESS Newswire / April 3, 2025 / Onco-Innovations Limited (CSE:ONCO)(OTCQB:ONNVF)(Frankfurt:W1H, WKN: A3EKSZ) ("Onco" or the "Company") is pleased to announce that its wholly owned subsidiary, Inka Health Corp. ("Inka Health"), which the Company acquired on or about February 3, 2025 (please see news release dated February 3, 2025), has now successfully completed analytical work under contract ("AZ Services Agreement") for AstraZeneca Canada ("AstraZeneca"), contributing to ongoing advancements in pharmaceutical evidence generation.

Commissioned by AstraZeneca in consideration for prescribed fees under the AZ Services Agreement (which was entered into on or about September 19, 2024), this work reflects Inka Health's expertise in developing rigorous methodologies to strengthen the reliability of real-world data in healthcare decision-making. By addressing key analytical challenges, the project has yielded insights with broad implications for regulatory evaluation of real-world evidence and market access strategies. As a result of this work, two poster abstracts[1] have been developed and will be presented at ISPOR 2025 in Montréal, showcasing key findings and their impact on the use of real-world evidence in pharmaceutical research.

The first study, titled "Addressing Bias and Generalizability Challenges in Non-Local Real-World Evidence Through Transportability Analyses"[2], was co-authored by Inka Health founders Paul Arora and Alind Gupta alongside AstraZeneca Canada. This research explores innovative methodologies to enhance the credibility and applicability of real-world evidence (RWE) in regulatory and market access decisions. RWE is data collected from everyday medical practice rather than controlled clinical trials, making it valuable but sometimes difficult to apply across different populations. It demonstrates how advanced analytical approaches, such as transportability analysis, can mitigate bias and improve the generalizability of international data, ensuring that findings from one country or setting can be adjusted to be more relevant for another. This can be particularly important for regulators and pharmaceutical companies seeking to make informed decisions on treatments across diverse healthcare systems.

The second study, "A Comprehensive Review of Real-World Evidence (RWE) Use in Submissions to Canada's Drug Agency (CDA)"[3], provides an in-depth evaluation of how RWE is utilized in regulatory submissions in Canada. Regulatory submissions are the formal applications pharmaceutical companies submit to health authorities when seeking approval for a new drug or therapy. Inka Health has identified key trends and future opportunities in leveraging RWE to support pharmaceutical decision-making. By analyzing past submissions, the study sheds light on how often and in what ways RWE has influenced drug approvals, helping to shape more efficient and evidence-based regulatory strategies. These findings highlight the growing role of data-driven insights in optimizing drug evaluation processes and regulatory strategies.