Key Considerations for Planning Complex Clinical Trials: An In-Depth Look into Oncology Trials

Life Sciences, Clinical Trials,
  • Thursday, September 01, 2022

Planning and optimizing complex clinical trials in oncology is challenging in an increasingly fast-paced environment. Knowing and understanding adaptive trial designs and master protocols such as basket, umbrella and platform trials, is critical toward accelerating clinical research.

In this session, endpoint’s featured speaker will share efficient clinical trial design strategies that expedite the development of oncology drugs and biologics and how leveraging technology is necessary for navigating today’s drivers of change.

Join this webinar to learn more about planning complex clinical trials in oncology.


Cat Hall, VP Data and Quality, endpoint Clinical

Cat Hall started her career as an academic Scientist in molecular and cellular before finishing her MBA and transitioning into pharmaceutical supply chain management. During her career, she developed notable expertise not only in clinical supplies but also in training development, process improvement, managing partnerships and the design and implementation of technologies such as IRT. She is well-known for focusing on bridging the GMP/GCP gap by bringing supply chain customer service through the last mile to patients. Cat joined endpoint in 2019 as VP of Product Strategy to help continue to bring the customer voice forward into shaping the future of IRT.

Message Presenter

Who Should Attend?

  • Outsourcing Management
  • Clinical Supply Chain Management
  • Clinical Trial Planning and Optimization Management
  • Clinical Operations Management

What You Will Learn

  • Industry insights into clinical oncology research
  • Understanding adaptive trial designs in oncology (platform, basket and umbrella)
  • What to consider and when to act when planning complex clinical trials
  • How to leverage advanced eClinical technology for multi-faceted protocols

Xtalks Partner


endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry.  For the past decade, their customer-obsessed team of professionals have been continuously evolving their suite of technologies to help Sponsors achieve clinical trial success.  Their dynamic IRT solution, PULSE ®, for patient randomization and management, site management, and drug supply management and leading-edge clinical supplies management tool, DRIVE, have proven to maximize the supply chain, minimize operational costs, and ensure timely and accurate patient dosing. endpoint is headquartered in the Boston area, with offices across the US, EU, and Asia.

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