Independence Blue CrossCommercial · Coverage · Medical Policy · PA · Genetics, Pediatrics, Internal Medicine +1 moreMedium impact
08.00.51l, Enzyme Replacement for the Treatment of Gaucher's Disease
Act
by Dec 31, 2024
Effective date
Jan 1, 2024
Identified
Jun 19, 2026
Summary
Independence Blue Cross removed its designated preferred product requirement for Gaucher's disease enzyme replacement therapy as of January 1, 2024. All three FDA-approved agents (imiglucerase/Cerezyme, taliglucerase alfa/Elelyso, and velaglucerase alfa/VPRIV) are now equally covered without preference, eliminating previous restrictions that favored VPRIV.
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01Billing team and prior authorization staff must update all internal policies, prior authorization templates, and billing system rules to remove any VPRIV preference language or requirement.
02Ensure claims for Cerezyme (J1786), Elelyso (J3060), and VPRIV (J3385) are processed equally without denial or step-therapy based on product selection.
03Remove any billing software logic that defaults to or requires VPRIV.
04Providers should be notified that all three agents are now interchangeable for coverage purposes as long as medical necessity criteria are met.
05Claims previously denied due to non-preferred product selection may be subject to appeals review.
Codes mentioned
J1786J3060J3385E75.22
Original notice
08.00.51l, Enzyme Replacement for the Treatment of Gaucher's Disease
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