Key Takeaways
- The CMS Cell and Gene Therapy Access Model could improve access to the products, but state participation remains unclear
- So far, only a handful of patients have received the treatment and its extensive requirements may mean it will go to only the most severe patients at first.
- If successful, the model could expand to include cell therapies in oncology or gene therapies in hemophilia B.
The manufacturers of two high-cost gene therapies for sickle cell disease recently agreed to participate in CMS’s Cell and Gene Therapy Access Model, which could allow the companies to more...
But it remains to be seen how many states will choose to participate in the voluntary program.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?