RETHINK CLINICAL TRIALS

Increase the success of your clinical program by connecting study data with real-world data at the patient level

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Insight

LEARN MORE FROM TRIALS

Better understand outliers and follow outcomes even after a study is complete

Flexibility

GAIN FLEXIBILITY

Answer the questions you didn’t think to ask when the trial was designed

Cut-Your-Cost

CUT YOUR COSTS

Reduce the need for site visits and lose fewer patients to follow-up

Partnering with Datavant has provided Parexel the ability to link disparate data sets to drive the complex analyses necessary for providing innovative scientific and clinical data strategies.

Jamie Macdonald

CEO, Parexel

Connect to the nation's largest ecosystem of real-world data to support:

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RETROSPECTIVE COHORT ANALYSIS

Understand study outliers and the outcomes of patients lost to follow-up

POST-MARKETING STUDIES

Lower the costs of monitoring for long-term safety and efficacy

HYBRID STUDIES

Join data collected through trials and RWD sources for a more holistic view of the patient

SYNTHETIC CONTROLS

Reduce time and costs by incorporating RWD sources and pragmatic design

How it Works

Datavant Patient Keys act as a unique, consistent ID that can be used to match a consenting patient’s study data to their data in the real world, without unblinding the study

How-It-Works

Datavant provides us with a broad array of built-in connections to real-world data sources, which can now be combined to yield a more holistic view of patient health than clinical trial data alone.

Dr. Michelle Longmire

CEO and Co-founder, Medable

Resources

White Paper
Trial Tokenization
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Webinar
Using RWD in Clinical Development
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White Paper
Datavant & Parexel Use RWD for Clinical Research
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Case Study
External Control Arms
Datavant External Control Arms
Contact us to Learn More