Webinar | March 29, 2022

Enriching Oncology Studies With RWD Before, During, And After the Trial

Source: Medable

The fragmentation of health data is one of the greatest challenges facing healthcare today. Patients have dozens of interactions with healthcare systems throughout their lives, and that information is retained in siloed databases across disparate institutions. With clinical trials being one of the most critical sources of evidence on drug effectiveness and safety, especially in oncology trials, it is imperative that we bridge the gap between clinical trial data and real-world data (RWD) to expand and extend trial value.

 In this webinar, experts from Medable, Datavant and Parexel discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes. By combining the power of a SaaS DCT platform with real-world data connectivity, therapies and new interventions can be approved faster and brought to market with higher fidelity evidence of their effectiveness and safety in a well-defined group of patients. This unlocks better outcomes, faster research, and healthcare at a lower cost.

 By linking RWD with clinical trial data, sponsors can:

  • Optimize protocol and study design by adding richer clinical details about the patient's health
  • Ensure appropriate trial continuation by explaining and understanding patient response
  • Differentiate with a safe and effective intervention by observing long-term effectiveness

Key Learning Objectives:

  • Simplify research by combining a decentralized clinical trial platform with the linkage of real-world data
  • Make the research experience frictionless for patients and sites by relieving them of the burden of clinic visits and manual data collection
  • Improve the quality and duration of evidence at a fraction of traditional trial costs

Who Should Attend:

  • Clinical Operations/Development, Oncology Leads, R&D, Study Management, Chief Medical Officers, Chief Scientific Officers, Medical Affairs at Large Pharma and Mid-Market Biotech
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