CHICAGO, Illinois – KMR Group, a leader in biopharmaceutical R&D performance analytics, completed the first of its kind Industry analysis on the comprehensive cost of clinical trials with a group of leading biopharma companies. The Clinical Trial Cost Study sets industry benchmarks, identifies statistically significant cost drivers and evaluates trial cost efficiency. As the cost of clinical trials continue to rise, the need for comprehensive cost performance data which accounts for both internal and external cost types has never been greater. With various methodologies for tracking and reporting cost, there has not been a comparable source for evaluating industry trial cost performance. As a primary objective of KMR Group’s Clinical Trial Cost Study, the analysis helps biopharma companies determine how much any given trial costs using a robust and systematic framework. Understanding the total costs of trials is only the first step in analyzing and assessing company performance. While any given company may tend to run more expensive trials, it is critical to understand why and how this can be improved. The KMR Group Study identifies statistically significant cost drivers which help explain the disparities across trials, prompting useful discussions and questions about trial design and operational plans. Another critical analysis performed as part of the Clinical Trial Cost Study focused on operational cost efficiency; helping companies address the question of whether their trials are more expensive than their peers when taking into account factors such as study size and disease. Once trials are normalized for these factors, companies can begin to assess those levers that drive cost in terms of how their own protocol design and trial execution choices as well as cycle time is impacting their efficiency. Trial Costs are comprised of personnel, outsourcing, expenses and grants; additionally taking into consideration a variety of factors e.g., company size, volume (subjects, sites, subject visits), strategic focus, resource strategy, geographic deployment and trial design. Any combination of cost types and cost factors can be assessed in an online application available to participants. The analysis helps companies gain insight into how expensive their trials are relative to peers as well as how efficient they are in executing their clinical trials in terms of cost. It helps companies identify areas of strength and weakness at a phase and therapeutic level. Importantly, the Study helps quantify cost savings based on improved Industry efficiencies, cycle times, and study design considerations e.g., study size. The Study’s methodology, which includes comprehensive clinical trials costs accounting for personnel, outsourcing, grants and expenses is what makes this particular analysis invaluable. “KMR Group’s Clinical Trial Cost methodology is impressive since it corrects for deficiencies in how companies track costs to trials. We apply rigorous standards to data collection at both trial and cost levels to ensure quality and confidence in the results,” commented Linda Martin, KMR Group President and Founder. About KMR KMR Group has worked exclusively in biopharmaceutical R&D since the early 1990s. KMR Group is an industry leader in benchmarking, analytics and performance management as well as a developer of on-line analytics tools that enable access to our propriety and rich datasets. KMR's clinical platform contains the most reliable source for trial performance, recruitment and site metrics data, with over 25,000 global clinical trials. Clients depend on these tools to benchmark performance, define recruitment strategies and shape enrollment plans and to identify best performing sites. For more information or for a demonstration of any of KMR's tools, please contact us. Visit our website at https://kmrgroup.com and follow us on Twitter @KMRGroupInc.
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Making the Grade: Registries as Sources of Regulatory-Grade Real-World Evidence (RWE)
February 13th 2025Dr. Peter Wahl, MLA, MS, ScD, VP and Global Head of Scientific Affairs at CorEvitas, part of the PPD™ clinical research business of Thermo Fisher Scientific, discusses the critical role of protocol-driven registries in generating regulatory grade RWE to serve multiple and evolving evidence needs across the drug development cycle. He covers key considerations for selecting the right type of registry, the advantages over EMR datasets, and how registry data contextualizes safety and effectiveness to fulfill FDA and EMA post-marketing requirements.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
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