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The New York State (NYS) Department of Health has applied to participate in the federal Centers for Medicare and Medicaid Services (CMS) Cell and Gene Therapy (CGT) Access model. The model is voluntary for State Medicaid programs and manufacturers and will test whether a CMS-led approach to developing outcomes-based agreements (OBAs) for cell and gene therapies increases Medicaid beneficiaries’ access to innovative treatment, improve health outcomes, and reduces health care costs to State Medicaid programs. The initial focus of the model is on gene therapies for people living with sickle cell disease, inclusive of Casgevy™ (exagamglogene autotemcel) and Lyfgenia® (lovotibeglogene autotemcel).
With CMS approval to participate in the CGT Access Model, and an effective date of January 1, 2026, NYS Medicaid providers should be aware of the following coverage guidelines:
Additional information is available on the CMS “CGT Access Model Frequently asked Questions” web page: https://www.cms.gov/cgt-access-model-frequently-asked-questions
Please review the State’s guidance in the October 2025 Medicaid Update. https://www.emedny.org/ProviderManuals/communications/PAD_update_-_10-24-25.pdf
Drug Claim Submission:
Providers may not use 340B inventory for the CGT Access Model drugs. Additional information for billing: the eMedNY New York State Medicaid General Professional Billing Guidelines, located at: https://www.emedny.org/providermanuals/allproviders/General_Billing_Guidelines_Professional.pdf.
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