Advancing Pediatric Platform Trials: A Conversation with Dr. Danny Benjamin

Podcast

Published: April 2024

Podcast Episode: Advancing Pediatric Platform Trials – A Conversation with Dr. Danny Benjamin

Recorded during the MRCT Center’s October 2024 conference, Advancing Pediatric Platform Trials: Streamlining Development, Maximizing Impact, this keynote conversation features Dr. Danny Benjamin, Kiser-Arena Distinguished Professor of Pediatrics at Duke University Medical Center.

Discussion Highlights:

  • The historical evolution of pediatric drug development and key regulatory milestones
  • The role and achievements of the Pediatric Trials Network (PTN)
  • How platform trials can increase efficiency and reduce burden in pediatric research
  • Ethical and operational challenges unique to pediatric platform trials
  • Real-world examples demonstrating the value of shared trial infrastructure
  • Future directions to drive innovation, collaboration, and regulatory alignment

🔗 Listen to the full episode: EP 1: Advancing Pediatric Platform Trials – A Conversation with Dr. Danny Benjamin

More about the Advancing Pediatric Platform Trials: Streamlining Development, Maximizing Impact conference:

The MRCT Center hosted a 2-day hybrid meeting in Washington DC in October 2024 to examine the potential benefits, challenges, and opportunities of platform trials for pediatric populations. In addition to consideration of overarching issues, three diseases – pediatric oncology, major depressive disorder (MDD), and multidrug-resistant tuberculosis (MDR-TB) – were chosen to represent different conditions, epidemiology, settings, therapeutic challenges, and patient populations, and to illuminate different potential approaches and solutions. 

With ~80 pediatric and platform trial experts from Europe, the UK, Asia, Australia and the US in attendance, the discussants were successfully identified knowledge gaps and practical challenges that impact pediatric platform trial planning and execution. Each of the three subgroups recommended actionable approaches to address identified issues, and the respective groups continued to meet and take concrete steps, furthering the momentum created at the workshop, with the MRCT Center remaining actively involved with each disease-specific subgroup to facilitate the next steps.

Podcast Episode 2: Trials Beyond Borders

Podcast

Episode 2 of the Trials Beyond Borders podcast is now available on all streaming platforms. In this episode, Racquel Bruton, Associate Director and Clinical Trials Diversity Portfolio Lead at Biogen, and Willyanne DeCormier Plosky, Program Director at the MRCT Center, discuss how sponsor companies are enhancing representation in clinical trials, particularly outside the US. Racquel highlights Biogen’s longstanding commitment to reaching underrepresented populations and explores how the MRCT Center’s roadmap can help organizations develop effective diversity action plans. Tune in to learn practical insights on operationalizing diversity strategies.

Podcast Episode 1: Trials Beyond Borders

Podcast

Presented on: August 28, 2024

The first podcast in our new series, “Trials Beyond Borders: Building Representative Clinical Trials Worldwide.” The podcast features a conversation with MRCT Center Program Director Willyanne DeCormier Plosky and Tinaya Gray, a consultant with ICON plc, focusing on communications between sponsors, CROs, and sites in planning for diversity action plans in the context of global trials.  

Related Resources

Global Representation
Model Diversity Action Plan (DAP)
Global GDEI Roadmap

Drug Researchers Refuse To Follow The Law. The Government Isn’t Stopping Them

Podcast

Broadcast on: January 24, 2020

Podcast: Science Friday

Before any new drug comes to market, it goes through a time-consuming process. Researchers have to recruit human subjects for a clinical trial, collect all the data, and analyze the results. All of that can take years to complete, but the end result could be worth it: a drug that treats a rare disease or improves patients lives with fewer side effects.

SciFri · Drug Researchers Refuse To Follow The Law. The Government Is Not Stopping Them.