Imaavy (nipocalimab)
Indications for Prior Authorization
Imaavy (nipocalimab)
-
For diagnosis of Generalized Myasthenia Gravis (gMG)
Indicated for the treatment of generalized myasthenia gravis(gMG) in adult and pediatric patients 12 years of age and older who are anti-acetylcholine receptor (AChR) or anti-muscle-specific tyrosine kinase (MuSK) antibody positive.
Criteria
Imaavy
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
For diagnosis of Generalized Myasthenia Gravis (gMG)
- Diagnosis of generalized myasthenia gravis (gMG) AND
- One of the following:
- Both of the following:
- Patient is anti-acetylcholine receptor (AChR) antibody positive AND
- One of the following: [2]
- Trial and failure, contraindication, or intolerance to two immunosuppressive therapies (e.g., glucocorticoids, azathioprine, cyclosporine, mycophenolate mofetil, methotrexate, tacrolimus) OR
- Both of the following:
- Trial and failure, contraindication, or intolerance to one immunosuppressive therapy (e.g., glucocorticoids, azathioprine, cyclosporine, mycophenolate mofetil, methotrexate, tacrolimus) AND
- Trial and failure, contraindication, or intolerance to one of the following:
- Chronic plasmapheresis or plasma exchange (PE)
- Intravenous immunoglobulin (IVIG)
- Both of the following:
- Patient is anti-muscle-specific tyrosine kinase (MuSK) antibody positive AND
- One of the following: [2]
- Trial and failure, contraindication, or intolerance to two immunosuppressive therapies (e.g., glucocorticoids, azathioprine, cyclosporine, mycophenolate mofetil, methotrexate, tacrolimus) OR
- Both of the following:
- Trial and failure, contraindication, or intolerance to one immunosuppressive therapy (e.g., glucocorticoids, azathioprine, cyclosporine, mycophenolate mofetil, methotrexate, tacrolimus) AND
- Trial and failure, contraindication, or intolerance to one of the following:
- Chronic plasmapheresis or plasma exchange (PE)
- Intravenous immunoglobulin (IVIG)
- Rituximab [3]
- Patient is 12 years of age or older AND
- Prescribed by or in consultation with a neurologist
Imaavy
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
For diagnosis of Generalized Myasthenia Gravis (gMG)
- Patient demonstrates positive clinical response to therapy
P & T Revisions
2025-07-02
References
- Imaavy Prescribing Information. Janssen Biotech, Inc. Horsham, PA 19044. April 2025.
- Sanders DB, Wolfe GI, Benatar M, et al. International consensus guidance for management of myasthenia gravis. Neurology. 2016;87(4):419-25.
- Alhaidar MK, Abumurad S, Soliven B, Rezania K. Current Treatment of Myasthenia Gravis. J Clin Med. 2022 Mar 14;11(6):1597.
Revision History
- 2025-07-02: New program.