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News and Events
Los Angeles County Modeling Updates
Since March 2020, Berry Consultants LLC has been collaborating with the Los Angeles County Department of Health Services to develop COVID-19 hospital demand modeling projections, utilizing an SEIR epidemiologic model to predict hospital needs and assess the impact of physical distancing measures, with their findings prominently featured in various media outlets.
Blog
DESIGNING A COLLECTION OF TRIALS
The article emphasizes the importance of optimizing clinical trial designs by investigating multiple therapies simultaneously and utilizing strategies like Bayesian thinking and platform trials to significantly reduce the time and resources needed to identify effective treatments for difficult medical conditions.
Blog
HYPOTHESIS TESTING, CLINICALLY IMPORTANT EFFECTS, AND DO WE PAY TOO MUCH FOR CLINICAL TRIAL INSURANCE?
Highly powered clinical trials are costly and often yield statistically significant but clinically meaningless results due to large sample sizes designed to mitigate random errors, suggesting the need for alternative approaches like flexible sample sizes and group sequential designs to optimize resource use and improve trial efficiency.
Blog
IMPROVING PROGRAM RESULTS THROUGH BETTER PHASE 1 AND 2 TRIALS
Kert Viele discusses the challenges and probabilities of success in a drug development program, highlighting that a standard approach often leads to a high rate of failure due to poor dose selection in early trials, but suggests that a revised strategy of continuous patient allocation and dose escalation can significantly improve the chances of successfully bringing an effective therapy to market.
Blog
WHEN SHOULD YOU BORROW HISTORICAL DATA (OR REAL-WORLD EVIDENCE)?
Kert Viele discusses the concept of historical borrowing in clinical trials, highlighting its potential benefits and risks, particularly in relation to FDA guidance and the importance of assessing "drift" to determine when it is appropriate to utilize historical control data for improving trial efficiency and accuracy.
Blog
HOW TO GET CONTROL? CONCURRENT VS CONTEMPORARY VS HISTORICAL VS SYNTHETIC CONTROLS
The discussion highlights the growing role of real-world evidence in clinical trials, particularly as a potential substitute for control arms, while emphasizing the need to address biases associated with various control methods and advocating for a future dominated by platform trials that balance cost savings with reduced bias risks.
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