About This Case Study
Acquiring patient insights for the design of clinical trials, prior to protocol implementation, can change the course of a study. Our client, a research and development executive at a major pharmaceutical company, surveyed Inspire members to improve the clinical trial protocol for a molecule meant to treat a severe respiratory condition.
1) Learn how foresight into barriers to participation can increase the opportunities for greater population inclusion.
2) Find out how obtaining actionable insights can improve clinical trial recruitment and retention.
3)Understand how patient insights can reduce screen failure rates, caused by consent withdrawal or patient non-compliance.
Download, “Improving Clinical Trial Protocol Design to Enhance Trial Participation”