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Rescue Study
Program Transition
Issue
Project rescue required due to prior CRO under performance and lack of experience to drive and achieve recruitment and enrollment goals
Sponsor
A leading global biopharmaceutical company.
Project
North American component of a 3-proto-col, phase 3 program involving 160 sites and 600 patients.
Solutions
– ProTrials built a robust transition plan for the outgo-ing CRO (as approved by the sponsor)
– Given our experience with study transitions, we had established tools, processes and leadership to address the specific needs
– Employed site-specific recruitment boosting tactics to ensure enrollment targets were met, e.g. ProTrials assistance with referral follow up, conduit between sites and recruitment vendor
– Established accountability by assigning a role of Recruitment Specialist
– Increased CRA responsiveness to site queries and challenges strengthened CRA-site relationships that led to sites meeting or exceeding study deliverable
Results
– Achieved 98%+ SDV rate two months in advance of client’s target
– Maintained 97%+ data entry rates across the program
– Visit report compliance in 2019 was 97%+ (with >800 VRs completed)
– ProTrials continues to build robust “Les-sons Learned” and “Best Practices” guid-ance documents that are shared with all transition study teams on an ongoing basis