Medical Benefit Updates – Advantage D-SNP
| Date: | October 13, 2026 |
| From: | Health Plan of San Joaquin/Mountain Valley Health Plan (“Health Plan”) Therapeutics Committee |
| To: | Health Plan Practitioners, Facilities, and Hospitals |
| Type: | Informational |
| Subject: | Medical Benefit Updates |
| Business: | Medicare Advantage D-SNP |
Effective December 21, 2026, the Pharmacy and Therapeutics Committee has approved the following changes to the medical benefit.
- CODE J8502- INJECTION, APONVIE, 1 MG: No PA required for Medi-Cal benefit. This code replaces code C9145 which was marked obsolete as of 4/1/26.
- CODE J3404 – INJECTION, ZOPAPOGENE IMADENOVEC-DRBA (PAPZIMEOS): PA required for Medi-Cal benefit. Reserved for patients who meet ALL of the following criteria:
- Age 18 years or older
- Histologically confirmed diagnosis of recurrent respiratory papillomatosis (RRP)
- Documented HPV (Human papillomavirus) serotype 6 or 11
- Prior to the very first dose, a surgical debulking procedure must be performed to remove visible papillomas and establish minimal residual disease
- Presence of laryngotracheal papillomas
- Patient has received or is planning to receive HPV vaccination, as indicated
• Limits: Maximum of 4 injections per treatment course. 1 course of treatment.
- CODE J2361 – INJECTION, DEPEMOKIMAB-ULAA, 1 MG (EXDENSUR): PA required for Medi-Cal benefit. Reserved for patients ages 12 and older, with poorly controlled, severe eosinophilic asthma with baseline serum eosinophil counts of either ≥ 150 cells/μL at initiation of treatment or ≥ 300 cells/μL in the past 12 months AND 2 or more exacerbations in the past 12 months, despite being compliant with dose-optimized [1] Medium to highdose Inhaled Corticosteroids (ICS) + [2] A second controller (e.g. LongActing Beta-2 Agonist (LABA), Long-Acting Muscarinic Antagonist (LAMA), leukotriene modifier, systemic corticosteroids). Must be prescribed by an allergist/pulmonologist. Exdensur must not be used as monotherapy. Must have tried and failed Nucala/Fasenra/Cinqair.
• Limits: None - CODE J2182 – INJECTION, MEPOLIZUMAB, 1 MG, CODE J0517 – INJECTION, BENRALIZUMAB, 1 MG, CODE J2786 – INJECTION, RESLIZUMAB, 1 MG, CODE J2356 – INJECTION, TEZEPELUMAB-EKKO, 1 MG: Adjust criteria definition for requirements in severe asthma to include medium-to-high-dose inhaled Corticosteroids (ICS). PA required for Medi-Cal benefit.
- CODE J2182 – INJECTION, MEPOLIZUMAB, 1 MG (Nucala): PA required for Medi-Cal benefit.
• For asthma: Nucala is reserved for patients ages 6 and older, with poorly controlled, severe eosinophilic asthma with baseline serum eosinophil counts of either ≥ 150 cells/μL at initiation of treatment or ≥ 300 cells/μL in the past 12 months AND 2 or more exacerbations in the past 12 months, despite being compliant with dose-optimized [1] medium-to-highdose Inhaled Corticosteroids (ICS) + [2] A second controller (e.g. Long-Acting Beta-2 Agonist (LABA), Long-Acting Muscarinic Antagonist (LAMA), leukotriene modifier, systemic corticosteroids). Must be prescribed by an allergist/pulmonologist. Nucala must not be used as monotherapy.
• For COPD: Nucala is reserved for adult patients with poorly controlled severe eosinophilic COPD with baseline serum eosinophil counts of either ≥ 150 cells/μL at initiation of treatment or ≥ 300 cells/μL in the past 12 months AND 2 or more moderate exacerbations or 1 severe exacerbation in the past 12 months, despite being compliant with doseoptimized triple therapy with [1] High-dose Inhaled Corticosteroids (ICS) + [2] A Long-Acting Beta-2 Agonist (LABA), and [3] Long-Acting Muscarinic Antagonist (LAMA). Must be prescribed by an allergist. Nucala must not be used as monotherapy.
• Limits: None - CODE J0517 – INJECTION, BENRALIZUMAB, 1 MG (FASENRA): PA required for Medi-Cal benefit. Reserved for patients ages 6 and older, with poorly controlled, severe eosinophilic asthma with baseline serum eosinophil counts of either ≥ 150 cells/μL at initiation of treatment or ≥ 300 cells/μL in the past 12 months AND 2 or more exacerbations in the past 12 months, despite being compliant with dose-optimized [1] medium-to-high-dose Inhaled Corticosteroids (ICS) + [2] A second controller (e.g. Long-Acting Beta-2 Agonist (LABA), Long-Acting Muscarinic Antagonist (LAMA), leukotriene modifier, systemic corticosteroids). Must be prescribed by an allergist/pulmonologist. Fasenra must not be used as monotherapy.
• Limits: None - CODE J2786 – INJECTION, RESLIZUMAB, 1 MG (CINQAIR): PA required for Medi-Cal benefit. Reserved for patients ages 18 and older, with poorly controlled, severe eosinophilic asthma with baseline serum eosinophil counts of either ≥ 150 cells/μL at initiation of treatment or ≥ 300 cells/μL in the past 12 months AND 2 or more exacerbations in the past 12 months, despite being compliant with dose-optimized [1] medium-to-high-dose Inhaled Corticosteroids (ICS) + [2] A second controller (e.g. Long-Acting Beta-2 Agonist (LABA), LongActing Muscarinic Antagonist (LAMA), leukotriene modifier, systemic corticosteroids). Must be prescribed by an allergist/pulmonologist. Cinqair must not be used as monotherapy.
• Limits: None - CODE J2356 – INJECTION, TEZEPELUMAB-EKKO, 1 MG (TEZSPIRE): PA required for Medi-Cal benefit. Reserved for patients ages 12 and older, with severe asthma AND 2 or more exacerbations in the past 12 months, despite being compliant with dose-optimized [1] medium-to-high-dose Inhaled Corticosteroids (ICS) + [2] A second controller (e.g. Long-Acting Beta-2 Agonist (LABA), Long-Acting Muscarinic Antagonist (LAMA), leukotriene modifier, systemic corticosteroids). Must be prescribed by an allergist/pulmonologist. Tezspire must not be used as monotherapy. Must not be used with anti-IgE, anti-IL4, or anti-IL5 monoclonal antibody agents.
• Limits: None
- CODE J2182 – INJECTION, MEPOLIZUMAB, 1 MG (Nucala): PA required for Medi-Cal benefit.
- CODE Q5168 – INJECTION, RANIBIZUMAB-LEYK, BIOSIMILAR, 0.1 MG (NUFYMCO), CODE J3490/J3590/C9399 – RANIBIZUMAB-HKDZ (RANLUSPEC): PA required for Medi-Cal benefit.
- Must meet ALL of the following:
- Eye condition appropriate for treatment, including:
- Diabetic macular edema ▪ Diabetic retinopathy
- Macular edema following retinal vein occlusion
- Myopic choroidal neovascularization
- Neovascular wet or exudative age-related macular degeneration
- Polypoid choroidal vasculopathy with active juxtafoveal or subfoveal lesions
- Indication approved by FDA or society guidelines
- No concurrent ocular or periocular infection
- Age 18 years or older
- AND must have failed or had clinically significant adverse effects to bevacizumab
- Limits: Limit one dose per eye every four weeks for ranibizumab injection and every 24 weeks (6 months) for Susvimo implant.
- Eye condition appropriate for treatment, including:
- Must meet ALL of the following:
- CODE J0178 – INJECTION, AFLIBERCEPT, 1 MG (EYLEA), CODE Q5147 – INJECTION, AFLIBERCEPT-AYYH (PAVBLU), BIOSIMILAR, 1 MG: Update to clarify bypass exceptions and to separate from Eylea HD. PA required for Medi-Cal benefit.
- Must meet ALL of the following:
- Eye condition appropriate for treatment, including:
- Diabetic macular edema, with or without diabetic retinopathy
- Macular edema following central or branch vein occlusion
- Neovascular (wet or exudative) age-related macular degeneration
- Indication approved by FDA or society guidelines
- No concurrent ocular or periocular infection
- Age 18 years or older
- AND must have failed or had clinically significant adverse effects to bevacizumab OR patient’s baseline visual acuity is 20/50 or worse with diabetic macular edema.
- Limits: Limit to standard dosing of one 2 mg dose per eye every 4 weeks.
- Eye condition appropriate for treatment, including:
- Must meet ALL of the following:
- CODE J0177 – INJECTION, AFLIBERCEPT HD, 1 MG (EYLEA HD): Update to criteria requiring trial of ranibizumab or aflibercept. PA required for Medi-Cal benefit.
- Must meet ALL of the following:
- Eye condition appropriate for treatment, including:
- Diabetic macular edema, with or without diabetic retinopathy
- Macular edema following central or branch vein occlusion
- Neovascular (wet or exudative) age-related macular degeneration
- Indication approved by FDA or society guidelines
- No concurrent ocular or periocular infection
- Age 18 years or older
- AND must have failed or had clinically significant adverse effects to ranibizumab or aflibercept.
- Eye condition appropriate for treatment, including:
- Limits:
- Limit to standard dosing of one 8 mg dose every 4 weeks for the first three (3) doses, followed by 8 mg once every 8 to 16 weeks (±1 week).
- Eylea HD maintenance dosing for every 4 weeks may only be approved for patients who have (1) documented initial response to the first 3-5 monthly doses and (2) documented loss of response following maintenance dosing of every 8 to 16 weeks.
- Limit to standard dosing of one 8 mg dose every 4 weeks for the first three (3) doses, followed by 8 mg once every 8 to 16 weeks (±1 week).
- Must meet ALL of the following:
- CODE J2777 – INJECTION, FARICIMAB-SVOA, 0.1 MG (VABYSMO): Update to criteria requiring trial of ranibizumab or aflibercept. PA required for Medi-Cal benefit.
- Must meet ALL of the following:
- Eye condition appropriate for treatment, including
- Neovascular (wet or exudative) age-related macular degeneration
- Diabetic macular edema, with or without diabetic retinopathy
- Indication approved by FDA or society guidelines
- No concurrent ocular or periocular infection
- Age 18 years or older
- AND must have failed or had clinically significant adverse effects to ranibizumab or aflibercept
- Limits: Does not exceed standard dosing per FDA package insert.
- Eye condition appropriate for treatment, including
- Must meet ALL of the following:
- CODE J0179 – INJECTION, BROLUCIZUMAB-DBLL, 1 MG (BEOVU): Update to criteria requiring ranibizumab or aflibercept. PA required for Medi-Cal benefit.
- Must meet ALL of the following:
- Eye condition appropriate for treatment, including
- Neovascular (wet or exudative) age-related macular degeneration
- Diabetic macular edema, with or without diabetic retinopathy
- Indication approved by FDA or society guidelines
- No concurrent ocular or periocular infection
- Age 18 years or older
- AND must have failed or had clinically significant adverse effects to ranibizumab or aflibercept
- Limits: Does not exceed standard dosing per FDA package insert.
- Eye condition appropriate for treatment, including
- Must meet ALL of the following:
- CODE J9119 – INJECTION, CEMIPLIMAB-RWLC, 1 MG: Medical necessity criteria will be applied. PA required for Medi-Cal benefit.
- CODE J9232 – INJECTION, DOCETAXEL (HOSPIRA), NOT THERAPEUTICALLY EQUIVALENT TO J9171, 1 MG: No PA required for Medi-Cal benefit. You may contact our Customer Service Department with any questions or concerns. For Medi-Cal only members: Monday through Friday, 8:00 am to 5:00 pm, at 1-888-936-7526 (PLAN), TDD/TTY 711.
If you have any further questions, please contact your Provider Services Representative, or call our Customer Service Department at 1-888-936-PLAN (7526). You may also visit https://www.hpsj.com/alerts/ for online access to the documents shared. The most recent information about Health Plan and our services is always available on our website www.hpsj-mvhp.org
