Applies to Employer plans.
Depends on your plan's benefitCovered only for select plans with specific benefit language allowing coverage of drugs for weight loss management or weight-related comorbidities; drugs for weight loss management are a standard exclusion for most benefit plans
Qualification pathways
You can qualify through any one of these.
MASH Initial Approval
All of:
- Member has a diagnosis of MASH with moderate to advanced liver fibrosis consistent with stages F2 to F3, confirmed by liver biopsy, FAST (FibroScan-AST), MAST (MRI-PDFF + MRE + AST), or MEFIB (MRE + FIB-4)
- Requested medication is prescribed by or in consultation with a gastroenterologist, hepatologist, cardiometabolic specialist, or primary care physician in consultation with any of the listed specialists
- Member does not have evidence of cirrhosis, hepatic decompensation, or hepatocellular carcinoma
- Requested medication will be used in conjunction with healthy lifestyle modifications (e.g., dietary or caloric restriction, exercise, behavioral support, community-based program)
MASH Continuation
All of:
- Member is requesting medication for continuation of therapy for MASH
- Member has achieved or maintained a positive clinical response (e.g., improvement in liver function such as reduction in ALT, reduction of liver fat content by imaging such as MRI-PDFF or FibroScan CAP)
- Member does not have evidence of cirrhosis, hepatic decompensation, or hepatocellular carcinoma
- Requested medication will be used in conjunction with healthy lifestyle modifications
Documentation to bring
- Chart notes or medical records documenting clinical findings supporting the diagnosis of MASH
- Documentation of liver fibrosis staging F2-F3 confirmed by liver biopsy, FAST score, MAST score, or MEFIB score
- Documentation that medication is prescribed by or in consultation with a gastroenterologist, hepatologist, cardiometabolic specialist, or PCP in consultation with listed specialists
- Documentation that member does not have evidence of cirrhosis, hepatic decompensation, or hepatocellular carcinoma
- Documentation of positive clinical response for continuation (e.g., reduction in ALT, reduction of liver fat by MRI-PDFF or FibroScan CAP)
Quantity limits
- All strengths — 4 pens
Approval and renewal
- Initial approval: 12 months
- Renewal: every 12 months
- Renewal: Member has achieved or maintained a positive clinical response (e.g., improvement in liver function such as reduction in ALT, reduction of liver fat content by imaging such as MRI-PDFF or FibroScan CAP). No re-verification of specialist prescribing or fibrosis confirmation methods required at continuation.
Not covered when
- Cirrhosis
- Hepatic decompensation
- Hepatocellular carcinoma
- Plans without specific benefit language allowing weight loss drug coverage
Policy note: MASH indication applies only to Wegovy (semaglutide injection), not Wegovy HD or Wegovy tablet (which are not listed under section VII). Fibrosis confirmation methods accepted: liver biopsy, FAST (FibroScan-AST), MAST (derived from MRI-PDFF + MRE + AST), and MEFIB (MRE combined with FIB-4 index). No lookback periods specified for confirmation tests. The T2DM exclusion that applies to weight loss and cv risk reduction indications does NOT apply to MASH. Quantity limit applies to injection formulation only; semaglutide tablet quantity limit is 30 tabs/30 days.
Policy effective May 19, 2026 · verified June 3, 2026 · source: Drugs For Weight Loss Management · View policy document (PDF)