ALTUVIIIO® [Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl] logo
Peer Mickey with quote “With 2 young daughters and a son running around at home, I could see the value of switching to ALTUVIIIO.”

Meet Mickey

“My family has a long history of hemophilia, so when I was born, they had me tested. I grew up with an uncle and older brother who also had severe hemophilia A. We lived in rural Ohio and knew we needed to be cautious but grew up with the same impulses and accidents as a lot of other kids.

In the ’70s and early ’80s our treatment options were limited. My uncle, my brother, and I all contracted HIV and hepatitis C because of the bad blood era. I’ve received treatments for both, and now neither can be detected in my blood.

In 1989, I started on a recombinant factor treatment, and that was the beginning of my prophy journey. It wasn’t everything I was looking for, but after being affected by blood-borne pathogens, I was scared to try new treatments. I infused with the same product for a long time before I was able and willing to ask for something new.

About 13 years ago, something changed for me. I learned about several different hemophilia communities and chapters near where I lived. It was eye-opening to meet people who had similar experiences to the ones I had. It was through the community that I first learned about ALTUVIIIO.

At my next appointment, my doctor confirmed that ALTUVIIIO showed a 48-hour half-life in adults. Together, we decided it was a good treatment option for me, and I started ALTUVIIIO in July 2024. I haven’t experienced any breakthrough bleeds since then.

One of the reasons I switched to ALTUVIIIO is that it’s easier for me to stick to my weekly prophy schedule. When I was on my prior treatment, I was supposed to infuse every 48 hours. With 3 busy kids, it was hard to keep up with that infusion schedule. Finding a treatment that allowed me to spend more time with my family doing the things that I love makes me feel empowered.”

Mickey is a promotional speaker compensated by Sanofi. Peer stories based on data collected March 2026.

Get an overview of all the Peers in our network here!

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INDICATION
INDICATION
IMPORTANT SAFETY INFORMATION
INDICATION

ALTUVIIIO® [antihemophilic factor (recombinant), Fc-VWF-XTEN fusion protein-ehtl] is an injectable medicine that is used to control and reduce the number of bleeding episodes in people with hemophilia A (congenital Factor VIII deficiency).

Your healthcare provider may give you ALTUVIIIO when you have surgery.

IMPORTANT SAFETY INFORMATION

What is the most important information I need to know about ALTUVIIIO?

Do not attempt to give yourself an injection unless you have been taught how by your healthcare provider or hemophilia center. You must carefully follow your healthcare provider’s instructions regarding the dose and schedule for injecting ALTUVIIIO so that your treatment will work best for you.

Who should not use ALTUVIIIO?

You should not use ALTUVIIIO if you have had an allergic reaction to it in the past.

What should I tell my healthcare provider before using ALTUVIIIO?

Tell your healthcare provider if you have had any medical problems, take any medications, including prescription and non-prescription medicines, supplements, or herbal medicines, are breastfeeding, or are pregnant or planning to become pregnant.

What are the possible side effects of ALTUVIIIO?

You can have an allergic reaction to ALTUVIIIO. Call your healthcare provider or emergency department right away if you have any of the following symptoms: difficulty breathing, chest tightness, swelling of the face, rash, or hives.

Your body can also make antibodies called “inhibitors” against ALTUVIIIO. This can stop ALTUVIIIO from working properly. Your healthcare provider may give you blood tests to check for inhibitors.

The common side effects of ALTUVIIIO are headache and joint pain.

These are not the only possible side effects of ALTUVIIIO. Tell your healthcare provider about any side effect that bothers you or does not go away.

MAT-US-2307222-v7.0-03/2026 Last Updated: March 2026