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Over 2 years in the XTEND-ed trial, a single dose of ALTUVOCT resolved:

A single dose

of bleeds in adolescents/adults2

of bleeds in children2

With excellent/good haemostatic response in 87.8% of adults/adolescents and 94.1% of children2,‡  
References

XTEND-ed is ongoing. Data cut: 21 February 2025. *For minor and moderate bleeding episodes occurring within 2–3 days after a prophylactic dose, a lower dose of 30 IU/kg dose may be used. Additional doses of 30 or 50 IU/kg every 2–3 days may be considered. For major bleeding, additional doses of 30 or 50 IU/kg every 2–3 days can be considered;1 

†For minor surgery, an additional dose of 30 or 50 IU/kg after 2–3 days may be considered. For major surgery, additional doses of 30 or 50 IU/kg every 2–3 days may be administered as clinically needed for perioperative management;1 

‡Assessment of response to ALTUVOCT treatment of individual bleeding episodes based on the ISTH 4-point response scale; §Investigators' or Surgeons' assessment of participant’s haemostatic response to ALTUVOCT treatment on the ISTH 4-point response for surgical procedures scale. AE, adverse event; ISTH, International Society on Thrombosis and Haemostasis; PwHA, people living with haemophilia A; TEAE, treatment emergent adverse event.

  1. Sobi . ALTUVOCT SmPC, 2026
  2. Susan S et al. Blood 2025;539-540


 

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