Cologuard®
Cologuard®, an Exact Sciences brand, provides FDA-approved noninvasive at-home colorectal cancer screening for U.S. adults 45+ at average risk. Its multi-target stool DNA technology has been used by over 20 million patients, distributed via telehealth, healthcare providers, and insurance partnerships.
- Company typePrivate
- Founded2014
- HeadquartersMadison, United States
- Headcount—
- GTM typeB2C
- OfferingHardware or Manufacturing
What Cologuard® does
Cologuard® is a commercial brand and product line of Exact Sciences Corporation (NASDAQ: EXAS) that develops and markets FDA-approved, noninvasive, at-home colorectal cancer screening tests for adults aged 45 and older at average risk. The core technology is a multi-target stool DNA (mt-sDNA) assay that detects both abnormal DNA markers and hemoglobin in a stool sample collected by the patient at home, eliminating the need for bowel preparation, sedation, or time off work associated with colonoscopy. The portfolio comprises the original Cologuard® test (FDA Pre-Market Approval, August 2014), which screens for 10 DNA markers plus blood with 92% overall colon cancer detection, and Cologuard Plus™ (FDA-approved 2024), a next-generation test using five optimized biomarkers with reported 95% colon cancer sensitivity and 99.98% negative predictive value.
Cologuard® firmographics
Firmographics- Name
- Cologuard®
- Legal name
- Exact Sciences Corporation
- Website
- https://cologuard.com
- Company type
- Private
- Founded year
- 2014
- Operating status
- Operating
- Short description
- Cologuard®, an Exact Sciences brand, provides FDA-approved noninvasive at-home colorectal cancer screening for U.S. adults 45+ at average risk. Its multi-target stool DNA technology has been used by over 20 million patients, distributed via telehealth, healthcare providers, and insurance partnerships.
- Ownership category
- akta.pro rank
Cologuard® industry classification
Industry- Product category
- Diagnostic Test Kits
- NAICS
- Medical Laboratories (621511), Medical and Diagnostic Laboratories (6215), In-Vitro Diagnostic Substance Manufacturing (325413)
- SIC
- In Vitro & In Vivo Diagnostic Substances (2835), Services-Medical Laboratories (8071)
- akta.pro primary industry
- Urinalysis & Routine Screening Diagnostics (HLAHAAAG)
- akta.pro secondary industry
- Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays) (HLAAAMAC)
Keywords
Where Cologuard® is headquartered
LocationHeadquarters
- HQ city
- Madison
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Cologuard® business model
Business model- GTM type
- B2C
- Offering type
- Hardware or Manufacturing
- Cost components
- Operations, Marketing or Sales, Technology or R&D, Personnel, Supply Chain
Revenue model
- Cologuard/Cologuard Plus Test Kits: Revenue generated from sale of FDA-approved colon cancer screening test kits. Most patients (96%) pay $0 due to insurance coverage including Medicare Part B and Medicaid. Self-pay price for Cologuard Plus is $599. Tests are also eligible for FSA, HSA, and HRA reimbursement.
- Laboratory Testing Services: Exact Sciences Laboratories processes all Cologuard tests at their CLIA-certified laboratory in Madison, WI. Revenue is generated when valid test results are produced and billed to insurance providers, Medicare, or self-pay patients.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| One time/ perpetual license | Pay-as-you-go | Insurance-covered screening for eligible adults 45+ |
| One time/ perpetual license | Pay-as-you-go | Self-pay option for Cologuard Plus |
Go-to-market motion2 records
Distribution channels3 records
Marketing channels5 records
Cologuard® product offering
Product offeringCore offering
Cologuard® manufactures and distributes FDA-approved, noninvasive, prescription-based, at-home stool collection test kits for colorectal cancer screening in adults aged 45 and older at average risk. The kits use proprietary multi-target stool DNA (mt-sDNA) technology to detect both abnormal DNA markers and blood in stool samples, and are processed at the company's CLIA-certified laboratory in Madison, Wisconsin, with results returned within 8–10 days.
Product overview
Cologuard® offers a portfolio of two FDA-approved, noninvasive, at-home colon cancer screening tests. The original Cologuard test (launched August 2014) detects 10 DNA markers and hemoglobin in stool samples, finding 92% of colon cancers. The newer Cologuard Plus™ test (next-generation, launched 2024) uses five optimized biomarkers for enhanced performance: 95% colon cancer detection, detection of 43% of advanced precancerous growths and 74% of high-risk lesions, with a 99.98% negative predictive value. Both tests are prescription-based, use a stool sample collection kit shipped to the patient's home, and are analyzed in Exact Sciences Laboratories with results returned within 8-10 days. The portfolio serves adults 45+ at average risk for colorectal cancer.
Differentiator
Problem solved
Functional benefit
Brands
- Cologuard Plus™: Next-generation FDA-approved colon cancer screening test with enhanced detection capabilities (95% colon cancer detection), optimized biomarkers, and reduced false positives compared to the original Cologuard test.
Products and services
- Cologuard® FDA-approved, noninvasive, prescription-based, use-at-home stool collection kit for screening adults 45+ at average risk for colorectal cancer. Detects 10 distinct DNA markers and hemoglobin (blood) in stool, with 92% overall colon cancer detection rate in clinical study. Results available in 8-10 days.
- Cologuard Plus™ Next-generation FDA-approved stool DNA test for colorectal cancer screening in adults 45+ at average risk. Uses five optimized biomarkers (DNA and blood) for improved detection: 95% sensitivity for colon cancer, 43% for advanced precancerous growths, 74% for high-risk lesions, and 99.98% negative predictive value. Covered by Medicare Part B with no copay or deductible.
Quantifiable outcome
- 92% of colon cancers detected overall; 94% of stage I & II colon cancers detected in clinical study of 10,000 participants
- +2 more outcomes
Companies that use Cologuard®
Customer profileNamed customers4 records
Segments4 records
Ideal customer profiles3 records
Cologuard® technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature3 records
Cologuard® partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- Recuro HealthcoreRecuro Health provides telehealth services enabling Cologuard ordering online. Patients complete a questionnaire through Recuro's platform and receive prescriptions from licensed telehealth providers, allowing direct-to-consumer online ordering of Cologuard kits. This partnership expands access to screening without requiring in-person healthcare visits.
Scale indicators7 records
Recent moves5 records
Expansion highlights4 records
Cologuard® competitors and assessment
Company assessmentEmerging players
- GRAIL: GRAIL's Galleri multi-cancer early detection test includes CRC signal detection alongside other cancers. While broader in scope, it competes for the same preventive-screening budget and patient population, particularly with health systems and employer wellness programs.
- Natera: Natera's Signatera and emerging oncology detection products address cancer screening and recurrence monitoring. While primarily focused on MRD, its oncology platform intersects with Cologuard's broader cancer-detection mission and target customer base.
- Universal Diagnostics: Universal Diagnostics is developing blood-based cancer screening tests, including CRC. It represents an emerging competitor in the noninvasive screening space that could overlap with Cologuard's target patient population if commercialized.
- Mainz Biomed: Mainz Biomed is developing ColoAlert, a stool-based molecular CRC screening test. It is a more regional / emerging competitor with similar core technology (stool DNA) targeting the same average-risk screening population as Cologuard.
Direct peers
- Geneoscopy: Geneoscopy's ColoSense is an FDA-approved stool-based RNA screening test for CRC. It directly competes with Cologuard in the same stool-sample, noninvasive CRC screening category and competes for the same provider prescriptions.
- Guardant Health: Guardant Health offers Shield, an FDA-approved blood-based colorectal cancer screening test. It competes directly with Cologuard for noninvasive CRC screening share, particularly with patients who prefer a blood draw over stool collection.
- Freenome: Freenome is developing a blood-based multiomics screening test for early CRC detection. It targets the same average-risk screening population as Cologuard and represents the next generation of noninvasive CRC screening competitors.
Others
- Polymedco: Polymedco manufactures OC-Auto FIT, one of the most widely used fecal immunochemical tests for CRC screening. It is an indirect competitor and adjacent technology provider competing for the same noninvasive CRC screening population through different modalities.
Broad incumbents
- Laboratory Corporation of America (Labcorp): Labcorp is a major clinical laboratory network offering FIT and other CRC screening services. As a broad incumbent, it competes with Cologuard through established health system relationships, complementary screening modalities, and in-office test options.
- Quest Diagnostics: Quest Diagnostics is a national reference laboratory offering FIT testing and other CRC screening diagnostics. It is a broad incumbent in the diagnostic lab space that competes for the same screening volume through different test modalities and health system contracts.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
Cologuard® social profiles
Digital presenceCologuard® compliance and trust
Trust signalCompliance3 records
Cologuard® financial estimates
Financial estimateRevenue estimate
Valuation estimate
Cologuard® leadership team
Management profileNumber of profiles
Profiles1 record
Cologuard® funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Cologuard® M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Cologuard®
What does Cologuard® do?
Cologuard® manufactures and distributes FDA-approved, noninvasive, prescription-based, at-home stool collection test kits for colorectal cancer screening in adults aged 45 and older at average risk. The kits use proprietary multi-target stool DNA (mt-sDNA) technology to detect both abnormal DNA markers and blood in stool samples, and are processed at the company's CLIA-certified laboratory in Madison, Wisconsin, with results returned within 8–10 days.
Is Cologuard® a public or private company?
Cologuard® is a private company. It is classified as public and is currently operating.
When was Cologuard® founded?
Cologuard® was founded in 2014.
Where is Cologuard® based?
Cologuard® is headquartered in Madison, United States, in the North America region.
How does Cologuard® make money?
Two revenue lines are on record. Cologuard/Cologuard Plus Test Kits are the primary driver. The others are laboratory Testing Services.
Who are Cologuard®'s main competitors?
Emerging players on record are GRAIL, Natera, Universal Diagnostics and Mainz Biomed. Direct peers are Geneoscopy, Guardant Health and Freenome. Polymedco is listed as an others. Broad incumbents are Laboratory Corporation of America (Labcorp) and Quest Diagnostics.
Does Cologuard® have an API?
No public API is recorded for Cologuard®.
What industry is Cologuard® in?
Cologuard®'s product category is Diagnostic Test Kits. Its primary akta.pro industry code is HLAHAAAG, Urinalysis & Routine Screening Diagnostics, with a secondary code of HLAAAMAC, Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays). Its NAICS code is 621511 and its SIC code is 2835.