Technology Leaders Join Forces to Bring Real World Evidence Data Analytics to Drug Development
NEW YORK, N.Y. and WALTHAM, M.A. – Medidata and SHYFT Analytics today announced a strategic commercial partnership to increase access to healthcare data analytics in clinical trials. The partnership will enable life sciences companies to add real world evidence (RWE) data from electronic medical records (EMRs) and health claims to information traditionally collected in clinical trials, providing a more comprehensive view of patient health. Using Medidata’s industry-leading clinical technology platform and SHYFT’s intelligent analytics, life sciences companies and their contract research organization (CRO) partners can analyze RWE data to improve study design and site selection, two of the most critical and costly components of successful drug development programs. The joint offering will provide insights that can be used to identify specific patient populations for studies across therapeutic areas, supporting efforts to design more effective protocols, more efficiently recruit study participants and uncover the best treatment paths in clinical practice. “As life sciences companies embark on more complex and targeted programs in oncology, rare diseases and a range of therapeutic areas, embedding real world evidence data and outcomes-based analytics early in the clinical trial process is imperative for success,” said Mike Capone, Medidata’s chief operating officer. “Our partnership with SHYFT is part of our ongoing efforts to help life sciences companies realize the value of data assets, providing the capabilities to overcome key R&D challenges and, in doing so, speed time to market and more quickly deliver new medicines to patients.” In working with more than 700 life sciences customers, Medidata has amassed among the largest sets of clinical data assets in the world. Combining the breadth and depth of Medidata’s clinical data with SHYFT’s real world evidence capabilities will provide the life sciences industry with unparalleled healthcare analytics. The partnership coincides with the recent completion of SHYFT’s Series B investment round, which included investments from Medidata, McKesson Ventures and other healthcare industry leaders. “This partnership represents an opportunity to leverage real world data and analytics to solve new and emerging challenges in clinical and drug-development activities,” added Zackary King, CEO and co-founder of SHYFT Analytics. “Customers can derive tremendous value from patient-centered data analytics and broaden its decision-driving utility across the enterprise. We’re excited to approach these challenges in partnership with Medidata and with a shared vision for advancing healthcare through analytics.” Founded in 2004, SHYFT helps life sciences companies integrate and translate different healthcare data sets into actionable insights. The company works with customers to integrate data from multiple third-party systems into its cloud platform, where the information is then delivered as personalized insights and analytics to clients across the clinical and commercial continuum.
Truqap Combination Shines in Phase III Trial for Prostate Cancer
November 26th 2024Data from the CAPItello-281 trial show Truqap alongside abiraterone and androgen deprivation therapy achieved a statistically significant and clinically meaningful improvement in radiographic progression-free survival.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.