Effective November 1, 2026: Pharmacy and Biopharmacy Policies
Date: 08/19/26
Ambetter from Superior HealthPlan, Ambetter Health (Solutions), and Superior HealthPlan (Medicaid) 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 November 1, 2026, at 12:00 AM.
Policy | Applicable Products | New Policy Overview or Updated Policy Revisions |
Ferric Carboxymaltose (Injectafer) (CP.PHAR.234) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Added redirection to generic for brand requests PER SDC request; added ICHRA line of business |
Emicizumab-kxwh (Hemlibra) (CP.PHAR.370) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Removed inhibitor level criterion for hemophilia with inhibitors; added bypassing agent option to on-demand usage that may be continued for hemophilia A with inhibitors; added ICHRA line of business. |
Teprotumumab (Tepezza) (CP.PHAR.465) | Ambetter, Ambetter Health | Added requirement that Tepezza is not prescribed concurrently with Lumvoa and member has not previously received Lumvoa; added ICHRA line of business. |
Concizumab-mtci (Alhemo) (CP.PHAR.625) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Removed inhibitor level criterion for hemophilia with inhibitors; revised provider confirmation of discontinuation of prophylaxis to exclusion for concurrent use of hemophilia prophylaxis agents with examples of allowable agents for on-demand usage; added ICHRA line of business. |
Fitusiran (Qfitlia) (CP.PHAR.706) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Added Hemlibra redirection for hemophilia A with SDC agreement; added template language of clinically significant adverse effects or contraindication for failure of bypassing agent, FVIII product, and FIX product as prophylaxis therapy; added bypassing agent option to on-demand usage that may be continued; added ICHRA line of business. |
Veligrotug (Lumvoa) (CP.PHAR.773) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | RT4: drug is now FDA-approved; modified to weight-based dosing per prescribing information; added requirement that member has not previously received Tepezza. |
Brepocitnib (CP.PHAR.793) | Ambetter, Ambetter Health | Policy created pre-emptively. |
Daraxonrasib (RMC-6236) (CP.PHAR.794) | Ambetter, Ambetter Health | Policy created pre-emptively. |
Venglustat (SAR402671) (CP.PHAR.795) | Ambetter, Ambetter Health | Policy created pre-emptively. |
Zilurgisertib (INCB0009258) (CP.PHAR.796) | Ambetter, Ambetter Health | Policy created pre-emptively. |
Cemdisiran (ALN-CC5) (CP.PHAR.797) | Ambetter, Ambetter Health, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Policy created pre-emptively. |
Ribitol (BBP-418) (CP.PHAR.798) | Ambetter, Ambetter Health | Policy created pre-emptively. |
Suzetrigine (Journavx) (CP.PMN.301) | Ambetter, Ambetter Health | Clarified failure of at least two analgesic medications to be within the last 30 days; added Journavx has not been prescribed within the last 30 days, or member is experiencing a new episode of moderate to severe acute pain; added tablet quantity limit of 29 tablets per 14 days per course of treatment; added total treatment duration of 14 days. |
Ensitrelvir (Xocova) (CP.PMN.311) | Ambetter, Ambetter Health | Policy created. |
Biologic and Non-biologic DMARDs (HIM.PA.SP60) | Ambetter | RT4: added newly FDA-approved Icotyde for PsO; for PsO: for Taltz and Icotyde pediatric redirection; updated criteria from “failure of TWO” to “failure of THREE” to align with redirection to Enbrel and Otezla as alternative option with “or” instead of “and” rationale; RT4: for Cosentyx, updated AS criteria with pediatric extension for ages 12 years and older per prescribing information; RT4: for Stelara/ustekinumab, updated CD criteria with pediatric extension for ages 2 to 17 years per prescribing information; RT4: for Hadlima, applied pediatric age extensions for HS and UV and added new single-dose autoinjector PushTouch dosage strength [80 mg/0.8 mL]; for HS, UC, UV, and continued therapy “All Other Indications In Section I”, added bypass of “FDA-approved age limit does not overlap” for preferred adalimumab biosimilar requirement; RT4: added FDA approved biosimilars Immgolis and Immgolis Intri to criteria; for RA for Simponi, Simponi Aria, Immgolis, and Immgolis Intri, added requirement for concomitant use with MTX or another DMARD; added HCPCS code Q5164. |
Benralizumab (Fasenra) (HIM.PA.SP70) | Ambetter, Ambetter Health | RT4: added criteria for newly approved indication of HES; |
Fidanacogene Elaparvovec-dzkt (Beqvez) (CP.PHAR.643) | Ambetter, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Retire, no longer commercialized. |
Valoctocogene Roxaparvovec-rvox (Roctavian) (CP.PHAR.466) | Ambetter, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP | Retire, no longer commercialized. |
To review all policies, please visit Superior’s Clinical, Payment & Pharmacy 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 the Centene Pharmacy Services (CPS) at 1-866-768-7147.