Skip to Main Content

Effective August 1, 2026: Pharmacy and Biopharmacy Policies

Date: 07/17/26

Ambetter from Superior HealthPlan, Ambetter Health Solutions, and Superior HealthPlan 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 August 1, 2026, at 12:00 AM.

Changes in these policies reflect preauthorization requirement amendments that are less burdensome to insureds, physicians, or health care providers.

Policy

Applicable Products

New Policy Overview or Updated Policy Revisions

Ranibizumab (Byooviz, Cimerli, Lucentis, Nufymco, Ranluspec, Susvimo) (CP.PHAR.186)

Ambetter,  Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP

Added Ranluspec to policy.

IncobotulinumtoxinA (Xeomin) (CP.PHAR.231)

Ambetter/ Ambetter Health Solutions, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP

Updated FDA approved indications to include coverage of pediatric patients for upper limb spasticity without regard for cerebral palsy etiology per PI.

Teplizumab-mzwv (Tzield) (CP.PHAR.492)

Ambetter/ Ambetter Health Solutions

Drug is now FDA approved for recently diagnosed Stage 3 T1D – updated criteria per FDA labeling: added upper age limit of 17 years and revised definition of recently diagnosed from 6 to 8 weeks; added new contraindication to Appendix C; added ICHRA line of business; references reviewed and updated.

Capivasertib (Truqap) (CP.PHAR.663)

Ambetter/ Ambetter Health Solutions

Added criteria for the newly approved prostate cancer indication; added ICHRA line of business.

Afamitresgene Autoleucel (Tecelra) (CP.PHAR.678)

Ambetter

Added pediatric extension down to 12 years of age and removed accelerated approval language per updated prescribing information.

Datopotamab deruxtecan-dlnk (Datroway) (CP.PHAR.715)

Ambetter/ Ambetter Health Solutions, Medicaid (STAR, STAR Health, STAR Kids, STAR+PLUS), and CHIP

Updated FDA approved indications to include additional use in adult patients with unresectable or metastatic TNBC who are not candidates for PD-1/PD-L1 inhibitor therapy; updated requirements for TNBC to allow use in PD-L1 negative tumors, and for PD-L1 positive tumors removed requirements for Combined Positive Score < 10 and disease is negative for germline BRCA 1/2 pathogenic variant and instead require provider attestation that member is ineligible for PD-1/PD-L1 inhibitor treatment.

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