


Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.
Alhemo is a novel prophylactic treatment for adult and pediatric patients aged 12 years and older with hemophilia A or B, specifically in those with inhibitors to FVIII or FIX. As a tissue factor pathway inhibitor (TFPI) antagonist, it works by modulating the clotting cascade to prevent bleeding episodes in these high-risk patients. Alhemo’s formulation, administered subcutaneously, ensures a regular dosing regimen with individualized adjustments based on plasma concentration levels.
This medication provides a vital therapeutic option for hemophilia patients who are resistant to traditional clotting factor treatments, offering hope for improved disease management and quality of life.
Alhemo(Concizumab) is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients aged 12 years and older with:
Hemophilia A (congenital factor VIII deficiency) with FVIII inhibitors;
Hemophilia B (congenital factor IX deficiency) with FIX inhibitors.
- Day 1: Loading dose of 1 mg/kg
- Day 2 and onwards: Once-daily dose of 0.2 mg/kg until the dose is individualized based on plasma concentration measurements.
After 4 weeks of treatment, plasma concentration of concizumab-mtci should be measured before the next dose using an enzyme-linked immunosorbent assay (ELISA).
