Model-based meta-analysis (MBMA) informs key drug development decisions by integrating data, published or unpublished, from multiple studies. Due to these various sources of information and large number of individuals, MBMA models require careful implementation, and this webinar will show you how to do it.

Using Monolix®, you will learn how to develop MBMA models from summary-level longitudinal data (e.g., mean responses over treatment arms), how to include between-study variability and between-treatment-arm variability, and how to apply appropriate weighting. The webinar will then show you how to use this model in Simulx® for decision support by simulating a clinical trial while accounting for variability in parameter estimates. With the step-by-step presentation of two case studies, you will discover practical applications of MonolixSuite™ to support model-informed drug development (MIDD).

Webinar is 1.5 hours.  Register now.

Date/Time: March 18, 2025 at 8:00 – 9:30 am PDT / 11:00 am – 12:30 pm EDT / 4:00-5:30 PM CET

Speaker:

• Chloé Bracis – Applications Manager, Clinical Pharmacology & Pharmacometrics Solutions

Q&A Panelists:

• Géraldine Cellière – VP Applications, Clinical Pharmacology & Pharmacometrics Solutions
  
• Amit Taneja – Director, Quantitative Clinical Pharmacology, Clinical Pharmacology & Pharmacometrics Solutions
  
• Yassine Lyauk – Associate Director, Clinical Pharmacology & Pharmacometrics Solutions