Pharmacist checking medicine bottle

How shorter clinical trial processes prolong the lives of patients

In this episode, Adlai Goldberg asks Tamie Joeckel, ICON’s Cell and Gene Therapy Global Business Lead, if an increased volume of CGT clinical trials with an accelerated process leads to more life-saving approvals.

There are 2,600 cell and gene therapy clinical trials taking place this year. In the US alone, this could translate up to 20 new therapy approvals in 2022, which presents a clear opportunity to make more life-saving therapies available to a greater number of individuals.

In this podcast, Tamie Joeckel – ICON’s Cell and Gene Therapy Global Business Lead – tells us what makes an increase in the volume of trials and an acceleration of the clinical trial process significant. She explains how doing so will allow diseases such as Alzheimer’s, Parkinson’s and diabetes to receive more focus.

Within the trials, the role of a sound digital strategy is at the forefront. In cell and gene therapy trials, 80% of data comes in within the first two months, compared with an even spread over years during a traditional trial. The need for an organized and effective strategy is paramount to make critical decisions. 

As the trials continue at speed, the knock-on effect also needs to be addressed. Supply chains models, manufacturing models and delivery models will need to evolve to ensure patients have access.

Despite the complexities involved, it’s a significant time in the life sciences sector. Even more so for Tamie. As a parent of a grown child with a rare disease, her mission is personal and emotive. With everything moving forward so encouragingly, she is optimistic and excited for the future.

Four things to take from the acceleration of cell and gene therapy clinical trials:

  • An accelerated clinical trials process means more trials are progressed, leading to an increased number making it to commercial availability.
  • There are challenges to overcome in regard to therapies reaching the patient – supply chain, manufacturing, delivery and, of course, cost.
  • The digital strategy within clinical trials must be sound. Incoming data must be organized to be fully effective.
  • COVID-19 led to trials becoming decentralized and for risk mitigation to be included in business continuity plans.

For your convenience, full text transcript of this podcast is also available. Read the transcript

Presenters

Photographic portrait of Tamie Joeckel
Tamie Joeckel
Cell and Gene Therapy Global Business Lead, ICON
Adlai Goldberg
EY Global Digital, Social and Commercial Innovation Life Sciences Leader

Podcast

Episode 03

Duration 29m 13s

In this series

Series overview
(Event List - Manual)

How shorter clinical trial processes prolong the lives of patients

In this episode, Adlai Goldberg asks Tamie Joeckel, ICON’s Cell and Gene Therapy Global Business Lead, if an increased volume of CGT clinical trials with an accelerated process leads to more life-saving approvals.
Podcast

Episode 03

Duration
29m 13s

Presenters

Tamie Joeckel

Cell and Gene Therapy Global Business Lead, ICON

Adlai Goldberg

EY Global Digital, Social and Commercial Innovation Life Sciences Leader

How digital solutions will help close the health equity gap

In this episode, Adlai Goldberg and two prominent chief medical officers explore and frame the health equity challenges the world is facing today.
Podcast

Episode 02

Duration
32m 49s

Presenters

The age of ‘Health Experience’

In this first episode of our EY Health Sciences and Wellness Experience podcast series, we explore the emerging and much needed age of “Health Experience.”
Podcast

Episode 01

Duration
08m 00s

Presenters

Pamela Spence

EY Global Health Sciences and Wellness Industry Leader and Life Sciences Industry Leader