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Hemophilia A Case Study: Henry


14 year old Caucasian male

Switched to ALTUVIIIO: July 2023

Henry, who has severe hemophilia A, enjoys playing baseball. He presented with a possible left-elbow bleed after waking up with pain and limited range of motion (inability to extend).

Patient Information

Presented with symptoms of a possible left-elbow bleed:

  • History of left-elbow bleeds, mostly relating to injury
  • No history of inhibitors
  • Henry’s last dose of factor-mimetic therapy was the day prior to presentation. No factor replacement therapy was infused

  • No surgeries

  • Brother and maternal grandfather have severe hemophilia A

  • BP: 122/86
  • HR: 71
  • Swelling and pain noted in left elbow

 

  • Inhibitor titer negative

Henry’s Path to High Sustained Factor Replacement Therapy, ALTUVIIIO

Diagnosis

  • Henry was diagnosed with severe hemophilia A (FVIII <1%) at birth

After diagnosis

  • At approximately 14 months old, Henry started SHL infusions 3x a week via a port
  • From 11 to 12 years old, he enjoyed playing baseball and switched to prophylaxis with factor-mimetic therapy and an on-demand SHL therapy
  • Throughout his childhood, Henry experienced multiple elbow bleeds (not considered a target joint)
    • At 14 years old, he experienced 1 left-elbow bleed and 1 left bicep muscle bleed secondary to an injury
    • He treated these injuries with an SHL therapy, received 4 weeks of physical therapy, and refrained from baseball for 4 weeks

Before ALTUVIIIO

  • After a 4-week hiatus from baseball, Henry participated in a baseball game and woke up the next day with pain and swelling in his left elbow
  • Henry presented to the HTC with a possible left-elbow bleed
  • Treatment regimen at the time: prophylaxis with factor-mimetic therapy and on-demand SHL therapy
  • Planned to treat bleed with on-demand ALTUVIIIO for 4 weeks while continuing factor-mimetic prophylaxis

Considering the switch

Henry, his parents, and his comprehensive care team discussed Henry’s:

  • Physical activity
  • Lifestyle goal to be on monotherapy

Together, they decided that switching to ALTUVIIIO would meet Henry’s treatment goals.

After ALTUVIIIO

Switched to ALTUVIIIO: July 2023 

  • Henry’s parents have been retrained on factor infusions
  • Since starting ALTUVIIIO prophylaxis, Henry has normal to near-normal Factor VIII levels (>40%) for >3 days of the week1 and has experienced 0 breakthrough bleeds

Do you have patients like Henry?

If so, it may be worth it to consider the following:

How good is good enough?
Would you consider a patient like Henry to be doing okay on their current treatment?

Choosing the right treatment
How would you discuss switching to a treatment option like ALTUVIIIO with patients like Henry?

Unlocking high sustained factor levels
Do you think high sustained factor levels and once-weekly dosing with ALTUVIIIO1 could benefit your patients like Henry?

BMI=body mass index; BP=blood pressure; FVIII=Factor VIII; HR=heart rate; HTC=hemophilia treatment center; SHL=standard half-life.

Other ALTUVIIIO patients who made the switch!

Meet Aaron

A 13 year old student and flag-football player with severe hemophilia A, previously on SHL prophylaxis therapy.

Meet Sean

A 39 year old technical support professional with severe hemophilia A who underwent a total knee arthroplasty.

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Learn how ALTUVIIIO was studied

The XTEND-1 trial studied ALTUVIIIO in the prophylaxis, on-demand, and perioperative settings in adult and adolescent patients.

What’s next?

If you’re interested in learning more about ALTUVIIIO, why not set up a chat with one of our representatives?

Indication

ALTUVIIIO® [antihemophilic factor (recombinant), Fc-VWF-XTEN fusion protein-ehtl] is a von Willebrand Factor (VWF) independent recombinant DNA-derived, Factor VIII concentrate indicated for use in adults and children with hemophilia A (congenital factor VIII deficiency) for:

  • Routine prophylaxis to reduce the frequency of bleeding episodes
  • On-demand treatment & control of bleeding episodes
  • Perioperative management of bleeding
Limitation of Use

ALTUVIIIO is not indicated for the treatment of von Willebrand disease.

Important Safety Information

Contraindications

ALTUVIIIO is contraindicated in patients who have had severe hypersensitivity reactions, including anaphylaxis, to the product or its excipients.

Warnings and Precautions
  • Allergic-type hypersensitivity reactions, including anaphylaxis, may occur with ALTUVIIIO. Allergic-type hypersensitivity reactions were not reported in the clinical trials. Advise patients to discontinue use of ALTUVIIIO if hypersensitivity symptoms occur and contact a physician and/or seek immediate emergency care.
  • Formation of neutralizing antibodies (inhibitors) to Factor VIII are possible following administration of ALTUVIIIO. Neutralizing antibodies were not reported in the clinical trials. Monitor all patients for the development of Factor VIII inhibitors by appropriate clinical observations and laboratory tests.
  • If assessment of plasma Factor VIII activity is needed, it is recommended to use a validated one-stage clotting assay. The ALTUVIIIO Factor VIII activity level is overestimated by the chromogenic assay and a specific ellagic acid-based aPTT reagent in one-stage clotting assay by approximately 2.5-fold. If these assays are used, divide the result by 2.5 to approximate the patient's ALTUVIIIO Factor VIII activity level.
Adverse Reactions

The most common adverse reactions (>10% of subjects) reported in clinical trials were headache and arthralgia.

Indication

Important Safety Information

Reference: 1. ALTUVIIIO Prescribing Information. Bioverativ Therapeutics Inc. Waltham, MA.

© 2025 Sanofi. All rights reserved. ALTUVIIIO, MyALTUVIIIO, and Sanofi are registered trademarks of Sanofi or an affiliate. MAT-US-2408466-v1.0-12/2024 Last Updated: December 2024