S T A T E O F N E W Y O R K
________________________________________________________________________
9360
2025-2026 Regular Sessions
I N A S S E M B L Y
December 19, 2025
___________
Introduced by M. of A. SANTABARBARA -- read once and referred to the
Committee on Health
AN ACT to amend the social services law, in relation to requiring Medi-
caid coverage of FDA-approved GLP-1 receptor agonist medications for
obesity, metabolic disorders, and autism-related compulsive eating
behaviors
THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND ASSEM-
BLY, DO ENACT AS FOLLOWS:
Section 1. Subdivision 2 of section 365-a of the social services law
is amended by adding a new paragraph (oo) to read as follows:
(OO) (I) FEDERAL FOOD AND DRUG ADMINISTRATION APPROVED GLP-1 RECEPTOR
AGONIST MEDICATIONS FOR THE FOLLOWING MEDICALLY INDICATED PURPOSES:
(1) OBESITY TREATMENT IN INDIVIDUALS WITH A BODY MASS INDEX OF THIRTY
OR GREATER, OR INDIVIDUALS WITH A BODY MASS INDEX OF TWENTY-SEVEN OR
GREATER WITH A RELATED COMORBIDITY;
(2) METABOLIC DISORDERS, INCLUDING PREDIABETES, TYPE TWO DIABETES AND
METABOLIC SYNDROME; AND
(3) CLINICALLY VERIFIED AUTISM-RELATED COMPULSIVE EATING BEHAVIORS
WITH CERTIFICATION FROM A QUALIFIED CLINICIAN, WHICH SHALL INCLUDE A
DEVELOPMENTAL PEDIATRICIAN, NEUROLOGIST, PSYCHIATRIST, PSYCHOLOGIST, OR
OTHER LICENSED PROVIDER.
(II) THE DEPARTMENT OF HEALTH IS AUTHORIZED TO REQUIRE THE FOLLOWING:
(1) STEP THERAPY PROTOCOLS FOR SUCH MEDICATIONS, WHERE CLINICALLY
APPROPRIATE;
(2) PRIOR AUTHORIZATION OF SUCH MEDICATIONS TO ENSURE MEDICAL NECESSI-
TY OF SUCH MEDICATIONS;
(3) INCOME-BASED ELIGIBILITY PRIORITIZATION FOR HIGH-NEED, LOW-INCOME
MEDICAID RECIPIENTS TO RECEIVE COVERAGE FOR SUCH MEDICATIONS; AND/OR
(4) DOCUMENTATION REQUIREMENTS FOR CLINICIAN CERTIFICATION IN CASES OF
AUTISM-RELATED NEED FOR SUCH MEDICATIONS PURSUANT TO CLAUSE THREE OF
SUBPARAGRAPH (I) OF THIS PARAGRAPH.
EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets
[ ] is old law to be omitted.
LBD14216-01-5
A. 9360 2
(III) THE DEPARTMENT OF HEALTH SHALL:
(1) DEVELOP CLEAR RULES AND CLINICAL CRITERIA FOR COVERAGE OF GLP-1
RECEPTOR AGONIST MEDICATIONS WITHIN ONE HUNDRED EIGHTY DAYS OF THE
EFFECTIVE DATE OF THIS PARAGRAPH;
(2) STREAMLINE PRIOR AUTHORIZATION FORMS AND TIMELINES;
(3) EVALUATE HEALTH OUTCOMES AND POTENTIAL MEDICAID COST SAVINGS
RELATED TO THE COVERAGE OF SUCH MEDICATIONS; AND
(4) SUBMIT AN ANNUAL REPORT TO THE LEGISLATURE DETAILING UTILIZATION,
COSTS AND MEASURABLE HEALTH OUTCOMES RELATED TO THE COVERAGE OF SUCH
MEDICATIONS.
(IV) THE PROVISIONS OF THIS PARAGRAPH SHALL APPLY TO GLP-1 RECEPTOR
AGONIST MEDICATIONS APPROVED BY THE FEDERAL FOOD AND DRUG ADMINISTRATION
ON OR BEFORE THE EFFECTIVE DATE OF THIS PARAGRAPH, AND SHALL ALSO APPLY
TO EMERGING GLP-1 RECEPTOR AGONIST MEDICATIONS AS SUCH MEDICATIONS ARE
APPROVED BY THE FEDERAL FOOD AND DRUG ADMINISTRATION AFTER THE EFFECTIVE
DATE OF THIS PARAGRAPH.
§ 2. This act shall take effect immediately.