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Gabriella Miller Kids First Research Act 2.0
3/13/2024, 11:47 AM
Summary of Bill S 1624
The bill is named after Gabriella Miller, a young girl who passed away from cancer at the age of 10. It seeks to honor her memory by increasing funding for research into childhood diseases and conditions.
Specifically, the Gabriella Miller Kids First Research Act 2.0 allocates $50 million annually for the next 10 years to the NIH Common Fund for pediatric research. This funding will support research on a wide range of pediatric health issues, including cancer, rare diseases, and other conditions that affect children. The bill also establishes a Pediatric Research Initiative Fund, which will provide grants to researchers studying pediatric diseases. Additionally, it requires the NIH to report to Congress on the progress and impact of the research funded by this legislation. Overall, the Gabriella Miller Kids First Research Act 2.0 aims to prioritize and support research that will improve the health and well-being of children across the United States. It has received bipartisan support in Congress and is seen as a positive step towards advancing pediatric medical research.
Congressional Summary of S 1624
Gabriella Miller Kids First Research Act 2.0
This bill modifies funding for, and requires reporting about, a pediatric disease research initiative within the National Institutes of Health (NIH).
Currently, this initiative receives funding through FY2023 from the 10-Year Pediatric Research Initiative Fund.
This bill directs certain penalties assessed by the Securities and Exchange Commission against pharmaceutical companies for specified violations to that fund. Additionally, the NIH must prioritize pediatric research that does not duplicate existing research activities when making allocations from the fund.
The bill also requires the Department of Health and Human Services to report to Congress about the research projects funded through the initiative.





