Altuviiio logo

Menu

Hemophilia A Case Study: Noah


2 year old Caucasian male

Switched to ALTUVIIIO July 2023
Noah, who has severe hemophilia A, presented for a comprehensive care visit. Noah’s mother wanted to feel confident in his bleed protection while he’s at daycare and she’s at work.

Patient Information

  • Around time of birth, Noah was started on SHL prophylaxis after prolonged bleed from heel stick and circumcision
  • From around 6 months of age, Noah was using weekly EHL therapy with SHL on-demand

  • Mild iron deficiency due to exclusive breastfeeding (using IV iron for treatment)

  • No family history of hemophilia A

  • Wt: 29 lbs
  • No significant findings on physical exam

 

  • Inhibitor titer negative
  • No joint bleeds detected in imaging

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

Diagnosis

Birth: Diagnosed with severe hemophilia A following uncontrolled bleeding from heel stick and circumcision

  • Was found to have a de novo mutation with no family history of hemophilia

After diagnosis

6 months old: Noah was initiated on extended half-life therapy and standard half-life therapy on demand.
2 years old: Noah is becoming increasingly physically active and is attending daycare.

Before ALTUVIIIO

  • Noah presented for a comprehensive care visit

Considering the switch

Provider and Noah’s mother discussed concerns about Noah’s:

  • Increasing physical activity
  • Need for proven bleed protection

Provider and Noah’s mother determined ALTUVIIIO was the optimal therapeutic choice to:

  • Provide bleed protection for Noah1

After ALTUVIIIO

Switched to ALTUVIIIO: July 2023 

  • Since switching to ALTUVIIIO, Noah has normal to near-normal Factor VIII levels (>40%) for ~3 days of the week. He has experienced 0 spontaneous bleeds and his mother now feels confident in his bleed protection1

Do you have patients like Noah?

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

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

Choosing the right treatment
How would you discuss switching to a more appropriate treatment option, like ALTUVIIIO, with patients like Noah?

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

EHL=extended half-life; FVIII=Factor VIII; IU=international unit; IV=intravenous; SHL=standard half-life; Wt=weight.

Other ALTUVIIIO patients that made the switch!

Meet Peter

A 32 year old reverend with severe hemophilia A previously on prophylaxis therapy.

Meet Otis

A 43 year old who works loading trucks and previously treated his moderate hemophilia A with an on-demand therapy.

shield icon

Safety from the pediatric study

Find out more about the ALTUVIIIO safety profile in the XTEND-Kids clinical trial.

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.

© 2024 Sanofi. All rights reserved. ALTUVIIIO, MyALTUVIIIO, and Sanofi are registered trademarks of Sanofi or an affiliate. MAT-US-2408466-v1.0-10/2024 Last Updated: October 2024