Benefits of Leveraging Real World Data (RWD) to Conduct Long-Term Follow Up

July 26, 2022
1:00 pm
Watch Now
Play button

Meet the speakers

Karma Rabon Stith
Global Oncology RWE COE Lead
Syneos Health
Robert Zambon
VP, Transformational Design
Andrew Mackinnon
VP & GM eConsent
Devin Gilliam
Business Development, Clinical Trials

About the webinar

Conducting long term follow up studies to ensure that life-saving therapies can be brought to patients safely is challenging. This places a burden on patients participating in the studies and operational challenges on life sciences study sponsors.

Connecting sources of real world data (RWD) to clinical trials data can create a more seamless process for conducting long-term follow up studies.

In this webinar, panelists will discuss how this approach enables many benefits, including the ability to:

  • Supplement data for patients lost to follow up
  • Augment trial data to help explain non-responders and adverse events

This approach can be particularly beneficial in specific therapeutic areas, including:

  • Cell and gene therapies: high regulatory burden (up to 15 years of data collection)
  • Oncology: endpoints such as overall survival can be assessed for Accelerated Approval
  • COVID-19: exploration of delayed adverse events

Achieve your boldest ambitions

Explore how Datavant can be your health data logistics partner.

Contact us