United States Representatives Diana DeGette (D-CO) and Fred Upton (R-MI), the lead authors of the 21st Century Cures Act, recently released their broad vision for a “Cures 2.0” and are soliciting feedback on the effort. Cures 2.0 is expected to broaden the landmark Cures Act and build upon the progress that has already been made since the passage of Cures.

Cures 2.0 is an effort to modernize coverage and access to life-saving treatments in the United States and across the world. The initiative is currently focused on hot-button issues such as digital health, the modernization and coverage of innovative treatments, the use of real-world evidence (RWE), and improving education and support for caregivers. One of the biggest focuses that would impact the Food and Drug Administration (FDA) seems to be a proposal to build on the RWE provisions in the original Cures Act – “We would like to build on our initial RWE work, both at FDA and across the federal health care landscape,” DeGette and Upton write in their request for feedback. They also want to improve coverage of digital health products and services by healthcare payers, including Medicare. “Digital technologies have helped to transform other sectors of the US economy in ways that improve access to products and services and decrease their costs without harming quality.

It is time for that same transformation to occur in health care,” DeGette and Upton write. 21st Century Cures Act A similar ask launched the initial 21st Century Cures Act campaign five years ago. The bipartisan duo of DeGette and Upton then spent two years crafting the bill and it was enacted in December 2016 and signed by President Barack Obama. That Act was focused on speeding up research and therapies for patients, bolstering aid to the National Institutes of Health (NIH), giving new powers and responsibilities to the FDA, and requiring more information sharing.

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