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Recruitment Optimization in Clinical Trials: Looking Towards an Adaptive Future
Session Chair(s)
Raviv Pryluk, PhD
PhaseV, United States
Recruitment is a significant building block of clinical trials and also one of the greatest challenges, often having a direct influence on trial success or failure. In-efficiencies associated with patient recruitment may lead to prolonged trial durations, increased costs, and delays in bringing effective treatments to market. This session will explore methods for predicting the effect of different recruitment patterns on trial progression, outcomes and likelihood of the trial to meet its goals and present newly available technologies and trial design measures for successfully advancing recruitment.
Learning Objective : Describe the considerations of recruitment rate optimization in clinical trials and adaptive trials in particular; Discuss the available technologies and methodologies for optimizing recruitment via dedicated software, patient advocacies, databases and registries and the evaluation of trade-offs between trial duration and sample size requirements within a variety of adaptive trial designs as compared with standard fixed designs.
Speaker(s)
Time is Life: Leveraging Innovation in Clinical Trials for Rapid Recruitment
Tanya Russell, PhD, MS, RPh
Pfizer Inc, United States
Vice President, Integration Lead
Potential for Leveraging AI/ML in Pre-Trial Recruitment Modelling
Jenny Higley, MS
Biogen, United States
Director, Head of Feasibility CoE
Harnessing the Power of Site Engagements Using Data-Driven Clinical Analytics
Sanghita Bhattacharya, PhD
Johnson & Johnson Innovative Medicine, United States
Associate Director Data Science , Feasibility and Analytics, Clinical Operations
Optimizing Clinical Trial Site Selection: Balancing Recruitment Efficiency and Population Diversity
Raviv Pryluk, PhD
PhaseV, United States
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