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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.
RT4: for Tofidence, added newly approved CRS indication to criteria; for CRS, revised criterion for CRS prophylaxis use to “administering T-cell engaging bispecific antibody therapy” and added option for CRS treatment related to T-cell engaging bispecific therapy per NCCN; removed criterion for “used as supportive care in severe CRS related to blinatumomab therapy” as requirement is met through criterion for CRS treatment related to T-cell engaging bispecific antibody therapy; for continued therapy, removed “CAR-T cell induced” as CRS also includes T-cell engaging bispecific antibody therapy; for CRS initial approval criteria and continued therapy, added “up to 4 doses total” for clarity and to align with Commercial and Medicaid; RT4: for Skyrizi, added newly approved pediatric extension for PsO and added redirection to Skyrizi for PsO pediatric ages; added new 55 mg/0.37 mL single-dose prefilled syringe dosage strength; RT4: for Skyrizi, added newly approved pediatric extension for PsA and added redirection to Skyrizi for PsA pediatric ages; for pJIA, removed Xeljanz XR; for PsO, added Tremfya requirement for initiating Stelara therapy for ages 6 to 17 years criteria to reflect pediatric extension; for PsA, added Tremfya and tofacitinib (generic Xeljanz) as requirement for initiating Stelara therapy for ages 6 to 17 years criteria to reflect pediatric extension. Per SDC: for RA, PsA, AS, pJIA, and UC, removed criteria requiring use of brand Xeljanz/Xeljanz XR and added criteria requiring use of tofacitinib/tofacitinib XR (generic Xeljanz/Xeljanz XR); added generic redirection to tofacitinib/tofacitinib XR for brand Xeljanz/Xeljanz XR requests.

Benralizumab (Fasenra) (HIM.PA.SP70)

Ambetter, Ambetter Health

RT4: added criteria for newly approved indication of HES;
added ICHRA line of business.

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