These flexible methods may be more appropriate than those initially designed for chemotherapy drug development.
TORONTO (PRWEB) October 17, 2022
As acceptance of flexible trial designs continues to advance, many sponsors are increasingly exploring alternate methods of dose escalation to support identification of a maximum tolerated dose (MTD) and recommended Phase II dose (RP2D) in open-label early phase or First-in-Human studies. Bayesian dose escalation designs have also coincided with advances in oncology therapy development, such as immunotherapies and antibody drug conjugates. These flexible methods may be more appropriate than those initially designed for chemotherapy drug development.
In this webinar, the featured speaker will discuss and cover: Common types of open-label adaptive dose escalation designs; Comparisons with rule-based designs; How to apply and use these designs in oncology therapy development; And how to determine which design is best suited for a clinical trial.
Register to learn the benefits of Bayesian dose escalation designs for oncology therapy development.
Join Vanessa Beddo, PhD, VP, Biostatistical Consulting, Allucent, for the live webinar on Monday, October 31, 2022, at 11am EDT (3pm GMT/UK).
For more information, or to register for this event, visit Benefits of Bayesian Dose Escalation Designs for Oncology Studies.
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