Bill119th Congress

S. 3302

Mikaela Naylon Give Kids a Chance Act of 2025

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Introduced
Dec 2, 2025
Origin Chamber
Senate
Policy Area
Health
Latest Action
Dec 2, 2025

Sponsor

Sen. Mullin, Markwayne [R-OK]

Republican·OK
Bioguide ID: M001190
First Name: Markwayne
Last Name: Mullin
By Request: N
37
Cosponsors
1
Committees
2
Actions
0
Amendments
3
Related Bills
0
Subjects
1
Summaries
3
Titles
1
Text Versions

Bill Details

Update Date
Apr 1, 2026
Origin Chamber
Senate
Bill Type
S
Bill Number
3,302
Congress
119
Introduced Date
Dec 2, 2025
Policy Area
Health
Is Law
No
Dec 2, 2025IntroReferral

Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Source: Senate

Dec 2, 2025IntroReferral10000

Introduced in Senate

Source: Library of Congress

Introduced in Senate· Dec 2, 20250

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.

Health, Education, Labor, and Pensions Committee

Senate· Standing

Introduced in Senate

Dec 2, 2025