Hympavzi (marstacimab-hncq)
Indications for Prior Authorization
Hympavzi (marstacimab-hncq)
-
For diagnosis of Prevention or to reduce the frequency of bleeding episodes
indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients 12 years of age and older with: 1) hemophilia A (congenital factor VIII deficiency) without factor VIII inhibitors, or 2) hemophilia B (congenital factor IX deficiency) without factor IX inhibitors.
Criteria
Hympavzi
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of one of the following:
- hemophilia A (congenital factor VIII deficiency) without factor VIII inhibitors
- hemophilia B (congenital factor IX deficiency) without factor IX inhibitors
- Drug will be used for prophylaxis to prevent or reduce the frequency of bleeding episodes AND
- Patient is 12 years of age or older AND
- Prescribed by or in consultation with a hematologist/oncologist AND
- One of the following: (applies to Hemophilia A only)
- For continuation of prior therapy OR
- Trial and inadequate response, intolerance, or contraindication to Hemlibra (emicizumab-kxwh)
Hympavzi
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Drug continues to be used for prophylaxis to prevent or reduce the frequency of bleeding episodes [A] AND
- Patient demonstrates positive clinical response to therapy (e.g., reduced bleeding episodes)
P & T Revisions
2025-04-02, 2025-01-08
References
- Hympavzi Prescribing Information. Division of Pfizer Inc. New York, NY. October 2024.
End Notes
- Do not use additional doses of HYMPAVZI to treat breakthrough bleeds. [1]
Revision History
- 2025-04-02: New Program
- 2025-01-08: New Program