MeCo Diagnostics is a venture-backed startup that has developed the only clinically validated test to match breast cancer patients to a breakthrough therapy, effectively unlocking a whole new treatment strategy.
Our landmark Phase 2 randomized controlled trial revealed the greatest survival benefit ever reported for a targeted therapy in the history of breast oncology:
We demonstrated a 62% reduction in risk of recurrence over 9.7 years on average for High MeCo Score patients, while Low MeCo Score patients experienced no benefit.
MeCo Diagnostics traces its origins to the oldest observation in cancer biology: tumors often grow stiffer than surrounding tissue, leading to a palpable lump. However, not all cancer cells are responsive to increased tumor stiffness, but those that are become “mechanically conditioned,” akin to deadly, microscopic machines that are programmed to wreak havoc as they spread throughout the body.
Fortunately, there is an FDA-approved antifibrotic drug which can be repurposed to deprogram these dangerous cancer cells. This serendipity has empowered us to develop a commercially viable, biomarker-enabled drug repurposing approach that synergizes with conventional neoadjuvant treatment.
Our lead asset, the MeCo Score, has been rigorously validated in 4 independent clinical studies of breast cancer comprised of over 4000 patients total, in partnership with oncologists at Cleveland Clinic, George Washington University, University of Arizona, and the Spanish National Cancer Research Center.
Moreover, since the MeCo Score matches patients to a generic-emergent drug, the cost of targeted antifibrotic therapy will soon be >10X cheaper than any other form of targeted therapy.
Since patients benefit from improved efficacy and payers benefit from reduced treatment costs, we are facilitating a win-win opportunity for healthcare stakeholders.
For more information, please reach out.
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所属行业
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生物技术研究
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规模
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2-10 人
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总部
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San Diego,California
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类型
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私人持股
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创立
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2022