Altuviiio logo

Menu

Hemophilia A Case Study: Aaron


13 year old Asian male

Switched to ALTUVIIIO: October 2023
Aaron, who has severe hemophilia A, presented for a comprehensive-care visit. Aaron maintains an active lifestyle, self-administers, and wanted to reduce the frequency of infusions.

Patient Information

Presented for a comprehensive care visit, with a desire to reduce the frequency of infusions while on twice-weekly EHL prophylaxis

  • Born in China (adopted in 2017); diagnosis history is unknown
  • Treated with SHL prophylaxis until early 2017 (dosing unknown)
  • Experienced possible right-ankle hemarthrosis while living in China (treatment unclear)

  • Surgical correction of VSD (2017)

  • Unknown, due to adoption

  • BP: 123/69
  • BMI: 19.22
  • HR: 64
  • No significant findings on physical exam

 

  • Inhibitor titer negative

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

Diagnosis

  • Aaron’s diagnosis history is unknown due to his adoption, but it was possibly due to right-ankle hemarthrosis while in China

After diagnosis

  • Aaron has tried both SHL and EHL therapies without complication, along with perioperative factor treatment
  • While in China, until 2017, he was on twice weekly SHL prophylaxis (dose unknown)
  • He switched to twice weekly EHL prophylaxis (40-50 IU/kg) in May 2017 upon adoption, with no reported joint or muscle bleeds while on EHL therapy
  • Aaron received perioperative EHL therapy in September 2017, 1000 IU prior to cardiac catheterization, and in November 2017, 1500 IU for 5 days starting on day of procedure for surgical correction of VSD (estimated patient weight was 83 pounds at the time of both procedures)

Before ALTUVIIIO

  • Aaron presented for comprehensive care visit
  • Possible history of right-ankle hemarthrosis while living in China but treatment is unclear
  • Treatment regimen: EHL prophylaxis, 40 to 50 IU/kg twice-weekly with excellent adherence

Considering the switch

The comprehensive care team, Aaron, and his family discussed Aaron’s:

  • Physical activity as a flag-football player at school
  • Desire to decrease infusion frequency
  • Desire for Factor VIII replacement therapy only

The care team, Aaron, and his family determined ALTUVIIIO was the best fit for him to:

  • Reduce infusion frequency1
  • Maintain Factor VIII levels closer to normal1

After ALTUVIIIO

Switched to ALTUVIIIO: October 2023 

  • Since starting ALTUVIIIO prophylaxis, Aaron has normal to near-normal Factor VIII1 levels (>40%) for >3 days of the week1 and has experienced 0 breakthrough bleeds

Do you have patients like Aaron?

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

How good is good enough?
Would you consider a patient like Aaron 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 Aaron?

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

BMI=body mass index; BP=blood pressure; EHL=extended half-life; HR=heart rate; IU=international unit; SHL=standard half-life; VSD=ventricular septal defect.

Other ALTUVIIIO patients who made the switch!

Meet Henry

A 14 year old student and avid baseball player with severe hemophilia A, previously treating with factor-mimetic prophylaxis and an on-demand SHL therapy.

Meet Sean

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

icon stonks

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

References: 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