Medicaid
Covered with requirementsWhat you need to qualify
- Age 18 and older
- Prescribed by or in consultation with a specialist
- Confirmed MASH diagnosis by FibroScan_VCTE, ELF_test, and liver_biopsy, fibrosis stage F2 to F3
- Not being used to treat type 1 diabetes
Qualification pathways
You can qualify through any one of these.
MASH — initial approval
All of:
- FDA approved indication of noncirrhotic MASH
- Member is 18 years of age or older
- Moderate-to-advanced liver fibrosis (stage F2 or F3) confirmed by at least one accepted method
- No chronic liver disease other than metabolic dysfunction-associated steatotic liver disease (MASLD)
- No T1DM or T2DM
- Metabolic comorbidities appropriately managed (T2DM, dyslipidemia, hypertension) as attested by prescriber
- Not using Wegovy in combination with other semaglutide-containing products or any GLP-1 receptor agonist
- Diet and exercise used in conjunction (clinical documentation required)
- Prescribed by or in consultation with gastroenterologist or hepatologist (or advanced care practitioner supervised by gastroenterologist or hepatologist)
Plus any one of:
- FibroScan with VCTE >= 8kPa and CAP >= 280dB/min
- ELF biochemical test score >= 9
- Liver biopsy showing stage F2 or F3 fibrosis with MASH
Documentation to bring
- Results of fibrosis confirmation test (FibroScan VCTE with VCTE >=8kPa and CAP >=280dB/min, OR ELF score >=9, OR liver biopsy showing F2 or F3 fibrosis with MASH)
- Clinical documentation (e.g., office notes) of diet and exercise discussion with member
- Prescriber attestation that metabolic comorbidities (T2DM, dyslipidemia, hypertension) are being appropriately managed
- Confirmation member does not have chronic liver disease other than MASLD
- Confirmation member does not have T1DM or T2DM
- Confirmation member will not use Wegovy in combination with other semaglutide-containing products or any GLP-1 receptor agonist
- Documentation that prescriber is or is in consultation with a gastroenterologist or hepatologist
Quantity limits
- all injection strengths — 4 pens per 28 days
Approval and renewal
- Initial approval: 2 months
- Renewal: every 12 months
- To renew, the plan looks for Member is tolerating maintenance dosing; member has not developed T1DM or T2DM; member is continuing a reduced calorie diet and increased physical activity in conjunction with Wegovy. Note: MASH diagnosis and fibrosis staging are not explicitly re-verified at continuation per the document and staying on a maintenance dose of at least 1.7 mg.
Not covered when
- Type 2 diabetes mellitus (T2DM excluded — member must not have T1DM or T2DM)
- Known liver cirrhosis (stage F4)
- Chronic liver disease other than MASLD
- Concurrent use with other semaglutide-containing products or any GLP-1 receptor agonist
- Obese members without MASH will not be approved
- Members who cannot tolerate dose escalation after additional 8-week approval will not be approved for continuation
- Wegovy should be discontinued if member cannot tolerate at least 1.7mg once weekly maintenance dosing
- Type 1 diabetes
Policy note: Initial approvals are for 8-week titration periods per dose; a separate PA must be submitted for each dose. An additional 8 weeks per dose may be approved for intolerable adverse effects during escalation with documentation. Subsequent (maintenance) approvals are for 1 year. FibroScan threshold for MASH is >=8kPa (vs >=8.5kPa for Rezdiffra criteria). The MASH indication criteria cover Wegovy injection only (not tablets). This document also requires a prior trial of Wegovy at maintenance dosing for at least 3 months as a step-therapy prerequisite for Rezdiffra (resmetirom) — but that is a step-therapy condition for Rezdiffra, not a Wegovy PA criterion. Last modified date on the Metabolic Disorders page is April 24, 2026.
verified June 4, 2026 · source: policy-385.html