News
Effective February 1, 2026: Pharmacy and Biopharmacy Policies
Date: 11/21/25
Magnolia Health Plan has added, updated or retired certain pharmacy and biopharmacy policies to ensure medical necessity review criteria is current and appropriate for members and the scope of services provided. As a result, the following policies are effective on February 1, 2026, at 12:00AM.
POLICY | APPLICABLE PRODUCTS | NEW POLICY OVERVIEW OR UPDATED POLICY REVISIONS |
Ruxolitinib (Jakafi, Opzelura) (CP.PHAR.98) | Ambetter | Policy updates include: · For atopic dermatitis, updated criteria with pediatric extension to include ages 2 years and older |
Immune Globulins (CP.PHAR.103) | Ambetter | Policy updates include: · For continued therapy, added language “(or health plan-preferred* immune globulin product)” to continue its usage, unless medical justification supports necessity for immune globulin product switch |
Aflibercept (Eylea, Eylea HD, Ahzantive, Enzeevu, Eydenzelt, Opuviz, Pavblu, Yesafili) (CP.PHAR.184) | Ambetter | Policy updates include: · Added new Eylea biosimilar Eydenzelt |
Factor VIII-von Willebrand (Alphanate, Humate-P, Vonvendi, Wilate) (CP.PHAR.216) | Ambetter | Policy updates include: · For Vonvendi, updated with pediatric extension for on-demand treatment of bleeding episodes, control of bleeding episodes, and perioperative management of bleeding, as well as with expansion to types 1 and 2 von Willebrand disease for routine prophylaxis |
Pembrolizumab, Pembrolizumab Berahyaluronidase alfa-pmph (Keytruda, Keytruda Qlex) (CP.PHAR.322) | Ambetter | Policy updates include: · Added new subcutaneous formulation Keytruda Qlex to policy · For Keytruda, converted Food and Drug Administration (FDA) approved indication for 400 mg every 6 week dosing regimen in adults with classical Hodgkin lymphoma and primary mediastinal large B-cell lymphoma to full approval |
Letermovir (Prevymis) (CP.PHAR.367) | Ambetter | Policy updates include: · Added criterion Prevymis must be initiated within 7 days post kidney transplant and 28 days post hematopoietic stem cell transplant |
Bortezomib (Boruzu, Velcade) (CP.PHAR.410) | Ambetter | Policy updates include: · Added new formulation Boruzu · Removed “if available” from generic bortezomib redirection as it is currently available |
Selumetinib (Koselugo) (CP.PHAR.464) | Ambetter | Policy updates include: · Revised criteria to reflect pediatric extension from age 2 years and older to age 1 year and older and added new dosage form (oral granules) with requirement for body surface area at least 0.4 m2 |
Lisocabtagene maraleucel (Breyanzi) (CP.PHAR.483) | Ambetter | Policy updates include: · Corrected follicular lymphoma and mantle cell lymphoma maximum dose from 100 to 110 x 106 chimeric antigen receptor (CAR)-positive viable T cells |
Beremagene Geperpavec (Vyjuvek) (CP.PHAR.592) | Ambetter | Policy updates include: · Removed lower age limit of 6 months and modified maximum dose from 1.6 and 3.2 x 109 PFU per week to 2 and 4 x 109 PFU per week per updated labeling · Added administration information allowing application by patient or caregiver per updated instructions for use |
Bedaquiline (Sirturo) (CP.PMN.212) | Ambetter | Policy updates include: · Updated to include pediatric extension down to 2 years of age and weighing at least 8 kg for multi-drug resistant tuberculosis without pretomanid per updated prescribing information |
Opioid Analgesics (HIM.PA.139) | Ambetter | Policy updates include: · Added criterion that request does not exceed health plan-approved quantity limit, if applicable to all indications |
Human Growth Hormone (Somapacitan, Somatrogon, Somatropin, Lonapegsomatropin-tcgd) (HIM.PA.161) | Ambetter | Policy updates include: · For Skytrofa, added new indication for replacement of endogenous growth hormone in adults with growth hormone deficiency and added new cartridge strengths (0.7 mg, 1.4 mg, 1.8 mg, 2.1 mg, 2.5 mg) |
Evinacumab-dgnb (Evkeeza) (HIM.PA.166) | Ambetter | Policy updates include: · Updated Food and Drug Administration (FDA) approved pediatric extension from at least 5 years to at least 1 years for homozygous familial hypercholesterolemia |
To review all policies, please visit Magnolia's Clinical & Payment Policies webpage.
Prior to updates, pharmacy and biopharmacy clinical policies are reviewed and approved by the Pharmacy and Therapeutics (P&T) Committee.
For questions or additional information, please contact Magnolia’s Pharmacy Department at 1-866-912-6285, ext. 66409.