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Our Clinical Areas of Focus
Phase II-IV Trials & Pharma sponsored led (RWE) Real World Evidence initiatives within outpatients clinics across North America
- ASCVD
- Obesity
- Elevated Lipoprotein (a)
- MASH
- Diabetes (Type I/II)
- Breast Cancer
- Lung Cancer
- Myocardial Infarction
- Congestive Heart Failure
- Hypertension
- Kidney Disease
- COPD
- Colorectal / GI Cancers
- Prostate Cancer
Multi AI Agents Built on Proprietary Data and Clinical Domain Expertise
Multi AI Agents Built on Proprietary Data and Clinical Domain Expertise
Why Customers Choose Us
Accuracy
Accuracy That Reduces Screen-Fails
Protocol-aligned patient identification delivers cleaner lists with fewer false positives—reducing screen-fails and re-work.
Speed
Speed That Accelerates Randomization
High-precision patient lists delivered in days enable faster site activation and quicker time-to-randomization.
Explainability
Explainability Clinicians Trust
Every patient match is transparent and traceable, enabling rapid validation by screeners, investigators, and monitors.
Stronger
Stronger Feasibility Outcomes
Accurate, explainable cohorts power more reliable feasibility studies and predictable enrollment performance.
Real-World Evidence (RWE) & Outcomes Programs
Beyond enrollment, Cardea helps sponsors and site networks generate real-world evidence from outpatient EMR data—supporting outcomes research, treatment pathway analyses, and care-gap measurement.
- Rapid cohort building from structured + unstructured EMR data
- Baseline characteristics, comorbidities, concomitant meds, lab trends
- Treatment pathways, persistence/adherence, outcomes, safety signals
- Site-level feasibility + retrospective analyses to de-risk trial planning
"Supporting RWE initiatives with sponsors including Novo Nordisk, Amgen, and Sanofi."
We Dramatically Reduce Our Client’s Patient Acquisition Cost (PAC)
Cardea delivers protocol-ready patient lists in record time— cutting pre-screening spend & accelerating enrollment.
Our Solution Provided
- 33 Day Advantage
- 50% Cost Reduction
Transforming Recruitment with a Purpose-Built Process
Transforming Recruitment with a Purpose-Built Process
Unparalleled Results
Speed
faster patient identification
Quality
Accuracy
Streamlining Clinical Trial
Pre-Screening for Optimal Recruitment
Eligible Patients Matches
These patients are matched by Cardea’s AI Agents and audited by our `Reviewer in the Loop’ against the full trial eligibility criteria.
Feasibility Study
Intended to help sponsors and site networks decide whether to proceed with trial setup at specific locations.
Supercharge your clinical trials
Risk free Patient recruitment
Shorter clinical trial period
improves reputation with sponsor
Nearly 80% of
trials fail to meet enrollment timelines
Increased trial criterion complexity
Limited access to relevant patient data
Inefficient screening process
High labor and/or Data extraction costs
Limited patient enrollment
Unparalleled Results
Speed
Quality
Accuracy
Supercharge your clinical trials
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With more than 250 Cardiometabolic terms, our
proprietary lexicon offers a comprehensive terminology base
Our innovative lexicon streamlines the pre-screening process for cardiometabolic clinical trials by significantly reducing manual data review and analysis. Utilizing advanced Natural Language Processing (NLP), it automates patient eligibility identification, allowing trial teams to quickly and accurately select candidates. This reduces time-consuming manual work and accelerates trial recruitment, helping studies meet enrollment goals faster and with greater precision.
Navigating Complex Pre-Screening, Simplified for You
Revolutionize your clinical trials and research with Cardea Health’s Proprietary Data Lake, designed specifically for an outpatient settings. Our solution empowers healthcare professionals to efficiently extract and leverage vital insights from unstructured data, ensuring unparalleled accuracy, speed, and cost-effectiveness. Simplify the process, we believe we will enable specialists to focus on delivering impactful results.
our value prop
Clinical Trials
Feasibility
Research
Optimization
- OCR
- NLP
- Etc: easy-to-understand
Our Approach to Privacy and Security
Our Trusted Partners




