S. 3302 · Where this bill is now
In committee
Introduced in the Senate, Dec 2, 2025
What this bill does
In plain words · AI-written from the official summaryOpens pathways for pediatric cancer drug trials
This bill makes it easier for researchers to test new cancer drugs in combination with drugs that are already approved and used to treat kids' cancers. It also extends the FDA's ability to give priority review vouchers (basically fast-track approval status) to companies developing treatments for rare pediatric diseases through 2030. The FDA will have to issue guidance on these changes and report back to Congress on how well they're working.
How it affects you
If you have a child with cancer, this bill may expand the treatment options available through clinical trials. Families dealing with rare pediatric diseases may also benefit from faster drug development and approval timelines. Most other people won't see a direct change, though the bill aims to help more kids access new cancer treatments more quickly.
Read the official summary (Introduced in Senate, Dec 2, 2025)
Mikaela Naylon 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, 2030. 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. 3302
A BILL
Mikaela Naylon Give Kids a Chance Act of 2025
Sponsor: Sen. Markwayne Mullin (R-OK) · Introduced Dec 2, 2025 · Health · 1 version of the text
Sources: Congress.gov actions and votes · bill text from GovInfo · latest official action Dec 2, 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