Hear from industry leaders and benchmark your strategies against experienced professionals including:

  • Bill-Prucka William Prucka, PhD
    Senior Research Scientist, Advanced Analytics - Clinical Trial Optimization
    Eli Lilly and Company
  • Mei-Chiung-Shih Mei-Chung Shih, PhD
    Assistant Professor of Biostatistics, Department of Health Research and Policy
    Stanford University
  • Junfang-Li Junfang Li
    Head of Biostatistics and Data Management
    Mitsubishi Tanabe Pharma America
  • KenLiu Kenneth Liu
    Associate Director
    Merck & Company

Examining the Successes and Pitfalls of Implementing and Utilizing Adaptive Clinical Trials

Pharmaceutical, biopharmaceutical, and biotech companies are increasingly implementing adaptive designs to reduce the length and cost of clinical trials, lower patient numbers, and improve the efficacy of their drug development process. With all its advantages, the successful execution of adaptive designs requires careful planning and coordination among teams of statisticians, data managers, regulatory affairs managers, clinicians, and drug supply and logistics managers. The 2nd Adaptive Designs for Clinical Drug Development will cover all aspects of the adaptive drug development process from design to implementation and management.

Benefit from industry presentations and case studies from companies such as Merck, Pfizer, Novartis, Roche, Eli Lilly, and many more. Gain the education, methodologies, and tools necessary for your development teams to collaborate, design, and implement successful adaptive trials. This conference promises to be a networking and discussion-filled event leaving you with new ideas and practical solutions to help you maximize the benefit of adaptive trials and reach the right answer the first time.

Who Will You Meet at the Conference?

Directors, Vice Presidents, Heads, Managers & Consultants specializing in:

  • Biostatistics
  • Clinical Development
  • Clinical Operations
  • Data Management
  • Regulatory Affairs
  • Clinical Research and Development
  • Drug Supply and Logistics
  • Clinical Pharmacy

Learn Best Practice Strategies on How to:

  • Implement adaptive designs in clinical setting
  • Reduce length and cost of clinical trials
  • Lower patient numbers and recruitment needs
  • Improve efficacy of drug development process
  • Improve patient response in-trial
  • Understand what questions to ask to ensure success

KEY TOPICS INCLUDE:

  • Implementing Adaptive Trials Across Your Portfolio
  • Ensuring the Compliance of Your Adaptive Clinical Trials
  • Coordinating Adaptive Trials With a CRO
  • Invoking Biomarkers to Streamline the Clinical Trials Process
  • Determining the Utility of Adaptive Trials
Media Partners
Animated_Media

[ Register Now ]