Improving Access And Support For Cell And Gene Therapies
Source: Cencora

In 2022, the FDA approved five new cell and gene therapies (CGT)—and approvals for new therapies are only expected to rise in the years to come. But although CGTs are potentially transformative, their effectiveness is undermined by difficulties with patient access and support, high costs, and a complex pathway to treatment.
Because these cutting-edge therapies require significant patient support, the onus is on sponsor companies, providers, and payers to coordinate care to improve patient access.
After reading this playbook, you’ll understand:
- The patient access problems that are inherent with CGTs
- The benefits of data collection and integrated patient support hubs for CGTs
- The importance of full buy-in and adoption by nurses, providers, payers, and sponsor companies
access the E-Book!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Cell & Gene? Subscribe today.
Subscribe to Cell & Gene
X
Subscribe to Cell & Gene
Cencora
This website uses cookies to ensure you get the best experience on our website. Learn more