S. 932 · Where this bill is now
In committee
Introduced in the Senate, Mar 11, 2025
What this bill does
In plain words · AI-written from the official summaryExpands pediatric cancer drug testing options
This bill makes it easier for researchers to test new cancer drugs in children by allowing studies that combine new drugs with ones already approved for treating pediatric or adult cancers. It also renews the FDA's program that gives priority review vouchers to companies developing treatments for rare diseases in children, which helps speed up the approval process for these medicines. The FDA will provide guidance on how to implement these changes and report back to Congress on progress.
How it affects you
Families with children who have cancer or rare pediatric diseases could eventually benefit from faster access to new treatment options. The changes mainly affect pharmaceutical companies and researchers working on pediatric drugs, but ultimately aim to get more treatment choices to sick children more quickly.
Read the official summary (Introduced in Senate, Mar 11, 2025)
Give Kids a Chance Act of 2025
This bill authorizes certain targeted clinical trials involving combinations of drugs to treat pediatric cancer, and renews the Food and Drug Administration’s (FDA’s) authority to award priority review vouchers (PRVs) to sponsors of new products for rare pediatric diseases.
Specifically, the bill modifies requirements relating to molecularly targeted pediatric cancer investigations to permit research on new drugs used in combination with active ingredients that have already been approved and that (1) have been determined to be part of the standard of care for treating a pediatric cancer, or (2) have been approved to treat an adult cancer and are directed at molecular targets for pediatric cancer.
The FDA must issue guidance on the implementation of these provisions and report to Congress on its efforts to ensure implementation. The Government Accountability Office (GAO) must report on the effectiveness of the bill's changes with respect to the development of pediatric cancer drugs.
The bill also renews the FDA’s authority to issue PRVs to sponsors of new products intended to treat rare pediatric diseases through September 30, 2029. This is known as the Rare Pediatric Disease PRV program. The program expired in December 2024.
GAO must report on the effectiveness of the Rare Pediatric Disease PRV program, including to what extent PRVs were successful in promoting drug development and expediting patient access to drugs for the treatment or prevention of rare pediatric diseases.
Written by AI (Claude) using only the official summary by the Congressional Research Service, the Library of Congress’s nonpartisan research staff. It can miss nuance, so check the official summary and the bill text for details.
1st SessionS. 932
A BILL
Give Kids a Chance Act of 2025
Sponsor: Sen. Markwayne Mullin (R-OK) · Introduced Mar 11, 2025 · Health · 1 version of the text
Sources: Congress.gov actions and votes · bill text from GovInfo · latest official action Mar 11, 2025: “Read twice and referred to the Committee on Health, Education, Labor, and Pensions.”
Sections
Sections · 3
- Sec. 1Short titleNo change
- Sec. 2Research into pediatric uses of drugs; additional authorities of Food and Drug Administration regarding molecularly targeted cancer drugsNo change
- Sec. 3Extension of authority to issue priority review vouchers to encourage treatments for rare pediatric diseasesNo change