Effective January 1, 2020, the following specialty drugs, which are eligible for coverage under the medical benefit for AmeriHealth New Jersey members, will require precertification:
- AscenivTM (immune globulin intravenous, human-slra) – Intravenous/subcutaneous immune globulin
- Esperoct® (antihemophilic factor [recombinant], glycopegylated-exei) – Hemophilia/coagulation factor
- Evenity® (romosozumab-aqqg) – Bone-modifying agent
- Eylea® (aflibercept) – Ophthalmic agents
- Herceptin HylectaTM (trastuzumab and hyaluronidase-oysk) – Antineoplastic agents
- Herzuma (trastuzumab-pkrb) – Antineoplastic agents
- KanjintiTM (trastuzumab-anns) – Antineoplastic agents
- Lucentis® (ranibizumab) – Ophthalmic agents
- Macugen (pegaptanib) – Ophthalmic agents
- Ontruzant® (trastuzumab-dttb) – Antineoplastic agents
- PolivyTM (polatuzumab vedotin-piiq) – Antineoplastic agents
- Revatio® (sildenafil) – Pulmonary arterial hypertension
- RuxienceTM (rituximab-pvvr) – Antineoplastic agents
- SynojoyntTM (sodium hyaluronate) – Hyaluronate acid products
- Trazimera (trastuzumab-qyyp) – Antineoplastic agents
- TriluronTM (sodium hyaluronate) – Hyaluronate acid products
- Tyvaso® (treprostinil) – Pulmonary arterial hypertension
- Ventavis® (iloprost) – Pulmonary arterial hypertension
- Xembify® (immune globulin subcutaneous, human-klhw) – Intravenous/subcutaneous immune globulin
- Zirabev (bevacizumab-bvzr) – Antineoplastic agents
In addition, the following drugs are currently pending approval from the U.S. Food and Drug Administration (FDA) and will require precertification for AmeriHealth New Jersey members once they receive FDA approval in 2020, or as of January 1, 2020, for any drug approved in 2019:
- abicipar – Ophthalmic agents
- brolucizumab – Ophthalmic agents
- casimersen – Duchenne muscular dystrophy
- cosyntropin depot – Endocrine/metabolic agents
- crizanlizumab – Miscellaneous therapeutic agents
- eptocog beta – Hemophilia/coagulation factors
- eptinezumab – Miscellaneous therapeutic agents
- givosiran – Miscellaneous therapeutic agents
- golodirsen – Duchenne muscular dystrophy
- isatuximab – Antineoplastic agents
- Lapelga (pegfilgrastim) – Colony-stimulating factor
- lisocabtagene maraleucel – Chimeric antigen receptor therapy
- margetuximab – Antineoplastic agents
- Reblozyl (luspatercept-aamt) – Miscellaneous therapeutic agents
- RVT-802 – Miscellaneous therapeutic agents
- viltolarsen – Duchenne muscular dystrophy
- Zynteglo (betibeglogene darolentivec) – Gene therapy
Lastly, the following drugs will no longer require precertification approval from AmeriHealth New Jersey as of January 1, 2020:
- Beleodaq® (belinostat) – Antineoplastic agents
- FolotynTM (pralatrexate) – Antineoplastic agents
- Imlygic® (talimogene laherparepvec) – Antineoplastic agents
- Istodax® (romidepsin) – Antineoplastic agents
- Monovisc® (high molecular weight hyaluronan) – Hyaluronate acid products
Learn more
In the absence of a published medical policy on any of these newly approved drugs, all requests will be subject to review in accordance with the FDA-approved indications and AmeriHealth New Jersey-recognized compendia.
These changes will be reflected in an updated precertification requirement list, which will be posted to our
website before these changes go into effect. The availability of the updated precertification list will be announced in a future Partners in Health UpdateSM article.