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Mainz Biomed (MYNZ) investor relations material
Mainz Biomed Registration Filing summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Registration Filing summary5 Dec, 2025
Company overview and business model
Develops and sells in-vitro diagnostic (IVD) tests for early cancer detection, with a focus on colorectal and pancreatic cancer.
Flagship product, ColoAlert, is CE-IVD certified and marketed in Europe; next-generation mRNA-based CRC screening test in development for US and EU launch.
Pursues partnerships with labs and technology firms to expand market reach and enhance product development.
Engaged in R&D projects, including PancAlert for pancreatic cancer, leveraging proprietary and licensed biomarkers.
Financial performance and metrics
Early revenue stage with ongoing operating losses since inception; profitability timeline uncertain.
Market value of outstanding ordinary shares held by non-affiliates as of December 5, 2025, was approximately $14.8 million.
$4.9 million of securities sold in the 12 months prior to the filing.
Use of proceeds and capital allocation
Net proceeds from securities sales intended for working capital purposes.
More detailed allocation and milestones to be provided in future prospectus supplements.
Impact of Quest Diagnostics partnership
PancAlert biomarker discovery strategy
Capital raising strategy given float limit?
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Next Mainz Biomed earnings date
H1 202529 Dec, 2025
Next Mainz Biomed earnings date
H1 202529 Dec, 2025
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Frequently asked questions
Mainz Biomed NV is a Germany-based molecular genetics diagnostic company focused on early detection of cancer. The company develops and commercializes in-vitro diagnostic tests, including non-invasive screening tools for colorectal cancer and other conditions. It operates in European and global markets with a focus on regulated clinical validation. The company is headquartered in Mainz, Germany, and its shares are listed on the NASDAQ.
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