01REQUIREMENTS:
By July 15, 2026 (before 8/1/2026 effective date):
- Billing team: Update billing system to remove age restrictions from Vyjuvek (J3401) coverage rules.
02System should now accept pediatric and adult claims of all ages when dystrophic epidermolysis bullosa diagnosis is present.
03- Billing team: Update Zolgensma (J3399) prior authorization templates to require provider documentation confirming member has NOT received prior gene therapy for spinal muscular atrophy (including Zolgensma or Itvisma).
04Flag claims without this documentation for denial.
05- Update encounter forms and clinical checklist in EMR to prompt providers for gene therapy history before Zolgensma ordering.
06By September 15, 2026 (before 10/1/2026 effective date):
- Billing team: Remove prior authorization requirement from Epioxa (J2789) billing rules.
07System should auto-approve claims when keratoconus diagnosis code is present; no manual PA review needed.
08- Billing team: Update Imaavy prior authorization criteria in system to require documentation of: MGFA Clinical Classification Class II-IV generalized myasthenia gravis, MG-ADL score ≥6, and refractory disease status.
09Request updated Medical Necessity Guidelines from Point32Health for specific refractory disease criteria.
10- Billing team: Add Vykoura to Medical Benefit Step Therapy logic.
11Configure system to require step therapy documentation per updated MNG.
12- Billing team: Update Targeted Immunomodulators coverage rules: Set Starjemza (ustekinumab-hmny) as preferred ustekinumab product.
13Configure system to require prior authorization denials for Yesintek unless documentation shows trial-and-failure of Starjemza or clinical rationale for continuation.
14- Billing team: Configure system to route all Adstiladrin (J9029) prior authorizations for Harvard Pilgrim Commercial and Tufts Medicare Preferred through OncoHealth vendor portal; discontinue internal PA review.
15Document OncoHealth contact information in billing team procedures.
16Consequences of inaction: Claims for Vyjuvek and Zolgensma without proper documentation will be denied.
17Epioxa claims will be improperly held for PA review.
18Imaavy authorizations may be denied for insufficient documentation.
19Yesintek claims may be approved inappropriately.
20Adstiladrin authorizations routed internally instead of OncoHealth will be delayed or denied.