CLINICAL RESEARCH

Accelerate & Optimize Clinical Trial Processes

Enhance and optimize your clinical trial starting with patient eligibility, stratification by social determinants of health SDOH and multiple patient variables. With HealthNexus™, you can control for comorbid conditions and select the optimal investigators and sites for your study.

Optimize Every Step of Your Clinical Trial

HealthNexus™ is a HIPAA-compliant platform that helps you optimize and enhance every step of your clinical trial – so you can accelerate the introduction of more innovative therapies to patients who need them most.

  • step

    Identify target patient populations

  • step

    Evaluate protocol assessment

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    Understand site feasibility

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    Identify patient & practice diversity

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    Determine optimal patient enrollment & track pharmacovigilance

  • Avoid delayed discovery of underlying conditions and factors that might render patients ineligible for your study
  • Bring your protocol assessments to the next level by understanding health disparities and predictability of outcomes with risk adjustment factors (RAF) and hierarchical conditions categories (HCC)
  • Identify health inequities and how practices compare for each provider’s patient census
  • Integrate the eligibility determination for optimal patient enrollment and PV tracking with HealthNexus™’ patient-level API

Reports

for Commercial Teams

  • Cohort Report
  • Experience & Overlap Report
  • HCP/HCO Provider Search Report

Start With a Finely Tuned Patient Cohort

Find the optimal patients for your study. Avoid the delayed discovery of underlying conditions, such as disease progression and other clinical factors that might render a patient ineligible for your trial. Develop a precise characterization of patient populations based on diagnosis (Dx), procedures (Px), prescriptions (Rx) and social determinants of health (SDOH). Iterate in real time based on varied criteria most likely to impact patient outcomes.

Evaluate Protocol Assessment

Bring your protocol assessment to the next level by understanding health disparities in the incidence, prevalence, mortality and burden of disease, as well as predictability of outcomes using Patient Risk Adjustment Factor (RAF) and Hierarchical Conditions Categories (HCC).

Understand Site Feasibility and Selection

Take action based on precise identification of investigators and sites that treat the patient population for your therapeutic area. Reporting is based on Dx, Px and Rx, enabling measurement of any “variability” of provider performance including risk-adjusted cost, quality scores (efficiency and effectiveness) — all to ensure the safest possible patient recruitment process.

All of their data comes linked and that is HUGE. A lof of companies struggle with that but this is PurpleLab™’s area of expertise.

Chief Commercial Officer, global network of life sciences and healthcare organizations

One platform. Endless possibilities to enhance and optimize your clinical trials.

If we want to obtain life-saving information and bring modern healthcare to everyone, we need to better leverage the data we have readily available. The key is making it easier to search by structurally and semantically harmonizing data from disparate sources – hard work the PurpleLab™ team has already done for you.

See How HealthNexus Works

HealthNexus™ data updates on an ongoing basis – not just once a year – and can easily integrate with your own RWD data. With complete, real-time insights at your fingertips, you can make better decisions for not only your clinical trial protocol but also the healthcare industry at large. See how by requesting a demo.