Cytel has launched East Bayes®, a web-based extension of the East® platform that enables adoption of computationally intensive Bayesian clinical trial designs.
East Bayes expands East Alloy’s functionality and computing power and integrates a selection of unique trial designs from Laiya Consulting’s renowned U-Design software. Through the new platform, customers will receive swift, easy access to a growing selection of advanced and innovative early-phase Bayesian dose-finding designs, all through a simple and intuitive graphical user interface. With easy adoption of designs such as i3+3, Multiple Cohort Expansion designs, and the Bayesian Logistic Regression Model, clinicians will now be able to more effectively identify optimal dosing, improve patient safety, and shorten clinical trials.
"Establishing a new therapeutic’s optimal dose is of utmost importance for maximizing chances of regulatory success. But the most advanced and flexible dose-finding designs have until now been off limits due to the complexity of the simulations required," said Yannis Jemiai, Chief Scientific Officer at Cytel. "East Bayes brings these complex mathematical models and algorithms smoothly and rapidly to clinicians in an accessible way, so now they can reap the benefits of Bayesian innovation confidently and autonomously."
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"The launch of East Bayes marks a new and exciting chapter for East – a platform that has been expanded with a continual stream of rich statistical know-how for more than 30 years. Many of the most innovative clinical trial designs available today were pioneered by the accomplished statisticians that created East. Further building on this tried and trusted platform allows us to continue connecting statisticians and clinicians to the fast-paced innovation that is reshaping modern pharmaceutical development," Priya Bhargava, Chief Product Officer at Cytel, said.