日期 2025 年 5 月 27 日
时间 11am ET
Model-Based Meta-Analysis (MBMA) has emerged as a powerful tool for integrating data across clinical trials and generating insights that efficiently inform drug development and regulatory decision-making. This webinar will unpack two distinct MBMA methodologies: modeling absolute outcomes and relative treatment effects.
Using a mix of simulated and real-world case studies, this webinar will cover:
- Choosing the Right Modeling Approach
When to apply absolute outcome vs. relative effect models based on clinical and development objectives. - Maximizing Impact with Covariates
Differentiating between prognostic and predictive covariates and how they influence model applications, plus best practices for covariate exploration. - Informing Decisions with Simulations
How MBMA-based simulations can improve trial design, support treatment comparisons, and guide go/no-go decisions. - Ensuring Model Credibility
Techniques for evaluating model fit and credibility to ensure reliable, decision-ready results. - Applying MBMA in the Real World
Case studies showing how MBMA informs regulatory submissions, product strategy, and development planning.
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Vice President, MBMA Capability Lead, Certara Drug Development Solutions
Matt advances the integration of published clinical outcomes data into development decisions and commercial and regulatory strategy via model-based meta-analysis (MBMA). Matt 与临床开发团队密切合作,确保在做出最关键决策的时候,能利用 MBMA 发挥最佳影响力。
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