Clinical Development | veranahealth.com

Clinical Development

Accelerate Your Clinical Research

Verana Health’s exclusive real-world data network and clinically true Qdata® can help accelerate clinical trials in ophthalmology and urology—from study startup through recruitment.

From protocol development and clinical trial design to site selection and identifying potential participants*, we help speed patient enrollment to help you meet your recruitment goals. Find out how Verana Health can support your next rare disease, site-based, or multi-disciplinary study.

4 of the Top 5 Pharmaceutical Companies Work with Verana Health on Clinical Trials

Verana Health Clinical Trial Offerings

Clinical Trial Design

Clinical Trial Site Selection

Utilize Verana Health’s exclusive Qdata to help refine your protocol design and patient cohort, including both patient and site feasibility analyses. Qdata is derived from exclusive speciality electronic health records (EHRs), so we can help you better understand whether a site will have patients who fit study criteria in near real-time. We can help you refine the inclusion and exclusion criteria to best meet your enrollment and study goals.

Leverage Verana Health’s exclusive Qdata to not just identify, but also engage clinical trial sites for your upcoming or ongoing study. Qdata contains variables that are key to site selection including: number of clinicians per practice, counts of complex procedures, generalized, de-identified patient demographics, and previous trial participation history. We can help you optimize for sites with trial experience and high patient volume in your indication of interest.

Patient Recruitment

Utilize Qdata to help locate practices with clinicians serving patients who fit your protocol inclusion and exclusion criteria. We will create a unique algorithm to apply to Qdata for your specific trial using both structured fields and unstructured physician notes to identify potentially eligible patients. Verana Health will then support site activation for eligible sites and activate Verana Health Trial Connect to identify potentially eligible patients to the clinicians and research staff treating those patients. Verana can help sponsors stay on top of the patient recruitment progress through our operational metrics and updates and leave the site support to Verana Health’s team.

Types of Clinical Trials Verana Health Supports

Rare Disease Trials

Verana Health can help practices match patients with rare conditions to relevant trials, and if eligible, offer them no-cost genetic testing and counseling.

Site-based Trials

Verana Health can help practices identify patients who match study inclusion and exclusion criteria, and to refer them to investigators at existing trial sites.

Our Customers

Verana Health is proud to collaborate with these leading Life Sciences organizations

Verana Health Supports Clinical Trial Teams Across Life Sciences

Clinical Development

Verana Health collaborates with Clinical Development teams across the drug or device lifecycle from phase one to four of the clinical program. We leverage real-world insights to help support your protocol development, clinical trial design, site feasibility and analysis, and can help identify potential participants for your study.

Clinical Operations

Verana Health works with Clinical Operations professionals to assist with trial design, site selection, site onboarding, and patient recruitment to accelerate trial delivery. We support teams as they design, plan and physically run trials using real-world evidence.

Contract Research Organizations

Verana Health collaborates with Contract Research Organizations (CROs) to accelerate study recruitment through site identification and patient enrollment leveraging tools such as Verana Trial Connect.

Verana Health Clinical Trials Case Studies

Trial Design

One of Verana Health’s clients was looking to understand the ideal profile of patients who would fit their study criteria including specific demographics, clinical characteristics, treatment patterns and outcomes. The client collaborated with Verana Health to leverage de-identified Qdata that was generated from structured fields and clinician EHR notes.

Trial Site Selection

One of Verana Health’s clients sought to develop therapies for unique manifestations of certain diseases. Verana Health helped the client leverage de-identified Qdata to identify specialty sites that may co-manage patients with these particular diseases, enabling the client to identify the most appropriate sites for their clinical trial.

Patient Recruitment

One of Verana Health’s clients was looking to find patients with a rare, inherited disease for their gene therapy clinical trial. They worked with Verana Health to leverage de-identified Qdata to help locate practices serving populations who fit the study criteria. Verana Health then conducted site outreach and worked with sites to ensure that potentially eligible patients were known to the clinical researchers. Practices then referred patients for genetic testing at no cost to the patients. Patients who were a fit for the trial were then referred to a study site.

Verana Health’s Clinical Trials By the Numbers

4 of Top 5

Life Sciences Companies are Customers

20K

Clinicians Participate in our RWD Network

~90M

De-identified Patients Included in our RWD Network

100

Peer-reviewed Studies Published Using Verana Health Data

3

Therapeutic Areas with Numerous Diseases

11

Years Longitudinal Data

*Data Current To: January 2025

Verana Health’s Therapeutic Areas

Ophthalmology

We partner with the American Academy of Ophthalmology and manage its IRIS®Registry (Intelligent Research in Sight) with more than 15,000 participating clinicians.

Urology

We partner with the American Urological Association and manage its AQUA Registry with more than 3,800 participating clinicians.