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Virtual

Apr 06, 2022 10:00 AM - Apr 08, 2022 5:00 PM

(US Eastern Standard Time)

DIA/FDA Biostatistics Industry and Regulator Forum

DIA Your Way! Join us virtually from the comfort of your home/office April 6-8 or watch later at a time that works for you. This event provides access to the materials for a full two months!

Session 4: Challenges in COVID-19 Vaccine Development for Adults and Pediatrics: A Journey from Clinical Trials to Real-World

Session Chair(s)

Shiowjen  Lee, PhD

Shiowjen Lee, PhD

Deputy Director, Division of Biostatistics, OBPV, CBER

FDA, United States

Satrajit  Roychoudhury, PhD

Satrajit Roychoudhury, PhD

Executive Director, Statistical Research and Innovation

Pfizer, Inc., United States

Vaccine development is a lengthy and expensive process. It typically takes multiple candidates and many years to produce a licensed vaccine. Conducting vaccine efficacy trials during an outbreak such as the COVID-19 pandemic poses unique challenges. It will generate simultaneous demand for vaccines around the world. Therefore, a strategic rollout plan for vaccines is required. An accelerated development plan requires innovations from all aspects of research and development including strategic design of clinical trials, defining clinical endpoints, and analyzing the study data. In addition, the development plan for the pediatric population will require additional safety considerations including the choice of appropriate dosing. This session will discuss the approval of vaccines and highlights issues with Covid-19 clinical development and rollout. It will compare the different issues with adult and pediatric development plans. Speakers will discuss the statistical challenges and solutions for the vaccine development and rollout plan.

Learning Objective :
  • Discuss FDA’s considerations for authorizing Covid-19 vaccines under
  • emergency use authorization (EUA) for pediatrics
  • Identify statistical issues, safety, and efficacy measures in the design of pediatric Covid-19 vaccine trials
  • Discuss potential statistical solutions to the uncertainty of developing vaccines
  • Discuss CDC considerations for a fast and effective rollout of the vaccine for the adult and pediatric population

Speaker(s)

John  Scott, PhD, MA

Speaker

John Scott, PhD, MA

FDA, United States

Division Director, Office of Biostatistics, CBER

Kenneth J. Koury, PhD

Speaker

Kenneth J. Koury, PhD

Pfizer, Inc., United States

Vice President, Head of Vaccine Clinical Research Biostatistics

Dean  Follmann, PhD

Speaker

Dean Follmann, PhD

National Institute of Allergy and Infectious Diseases, United States

Assistant Director for Biostatistics; NIAID Chief Biostatistics Research Branch

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