Transforming The Future of Cancer Detection with Biomarker Blood Tests
Transforming the Future of Cancer Detection
Cizzle Bio is driving a new era in cancer diagnostics, empowering patients and physicians with early-detection biomarker blood tests for cancer developed by the world’s leading experts. Our flagship test, the CIZ1B Biomarker Blood Test for Lung Cancer, is a leading-edge breakthrough in minimally invasive, highly accurate early detection for the world’s deadliest cancer.
Cizzle Bio is driving a new era in cancer diagnostics, empowering patients and physicians with early-detection biomarker blood tests for cancer developed by the world’s leading experts. Our flagship test, the CIZ1B Biomarker Blood Test for Lung Cancer, is a leading-edge breakthrough in minimally invasive, highly accurate early detection for the world’s deadliest cancer.
PROBLEMDetect Early. Save Lives.
Cancer is one of the leading causes of death worldwide, and late detection drastically reduces survival rates. The need for accurate, cost-effective, early-detection tools has never been more urgent.
LUNG CANCERNearly 5,000 lives are lost daily, with 75% of cases diagnosed at advanced stages, when treatment options are limited, and survival rates are low. 1
EARLY DETECTION IS KEYIdentifying cancer at its earliest stages significantly improves survival rates, giving patients hope for a better future.
The Urgency of Early Detection
Lung cancer is known for its silent progression, often remaining undetected until late stages when treatment options are limited. While early detection is vital to improve cancer survival, only a fraction of high-risk individuals receive routine testing.
LUNG CANCERSCREENING RATESFewer than 6% of the 14.2 million Americans recommended for annual screening undergo testing, leaving millions undiagnosed. 3
SOLUTIONA Revolutionary Biomarker Blood Test
Cizzle Bio leverages cutting-edge biomarker technology to provide a minimally invasive, highly accurate blood test for early lung cancer detection.
CIZ1B
Biomarker Test for Early Detection of Lung Cancer
Sensitivity
NPV
- Sensitivity of 95% for Stage I Detection and Negative Predictive Value (NPV) at 96%. 4
- A minimally invasive, cost-effective tool that minimizes need for repeated CT scans—reducing false positives, unnecessary follow-ups, and radiation exposure.
Partnering with Industry Leaders
In collaborating with industry leaders like Moffitt Cancer Center and BBI Solutions, our work is driven by trusted partnerships and cutting-edge research. Together, we’re integrating minimally invasive biomarker blood tests into mainstream healthcare.
Saving Lives, One Test at a Time
At Cizzle Bio, our driving purpose—Detect Early. Save Lives.—inspires every breakthrough we deliver. By giving patients the power of early action and equipping physicians with precision diagnostics, we’re changing the course of cancer care and saving more lives.
FOR PATIENTS
Take proactive steps.
Learn how to get tested.
Learn More
FOR PHYSICIANS
Learn more about how to access our CIZ1B Biomarker Blood Test for Lung Cancer.
Learn More
Join us in the fight against cancer.
Help us change these dire statistics. Stay informed and support advancements in cancer diagnostics. Subscribe for updates.
References:
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Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021 May;71(3):209-249.)
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Sung, H., Ferlay, J., Siegel, R. L., Laversanne, M., Soerjomataram, I., Jemal, A., & Bray, F. (2021). Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: A Cancer Journal for Clinicians, 71(3), 209-249
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American Lung Association. (2024). State of lung cancer: Key findings. Retrieved October 26, 2025, from https://www.lung.org/research/state-of-lung-cancer/key-findings
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Coverley D, Higgins G, West D, et al. A quantitative immunoassay for the lung-cancer biomarker CIZ1b in patient plasma. Clin Biochem. 2017;50(6):336-343.