What is ADVATE?

ADVATE is a medicine used to replace clotting factor (factor VIII or antihemophilic factor) that is missing in people with hemophilia A (also called “classic” hemophilia). ADVATE is used to prevent and control bleeding in adults and children (0-16 years) with hemophilia A. Your healthcare provider (HCP) may give you ADVATE when you have surgery. ADVATE can reduce the number of bleeding episodes in adults and children (0-16 years) when used regularly (prophylaxis). ADVATE is not used to treat von Willebrand disease.1

In the hemophilia A community, no two patients are the same

When finding a factor VIII deficiency bleeding disorder treatment for hemophilia A, you and your healthcare provider should consider your individual needs.1 There are many characteristics that make you unique.1,2

Each patient with hemophilia A is unique and has different needs, lifestyle, bleed frequency, and personal goals. ADVATE [Antihemophilic Factor (Recombinant)] is a treatment option for hemophilia A.

While living with hemophilia A will always be a part of your reality—both the welcome and unwelcome moments—you need treatment options that can help navigate the complexities of real life with hemophilia A.

What is a bleeding phenotype?

A patient’s bleeding phenotype is a collection of his or her bleed history, including bleeding disorder type and severity, annual bleed frequency, and overall joint health.3

What is PK?

Pharmacokinetics (or “PK”) is the science of how a drug is used up in the body.4 A person's PK profile helps determine how quickly or slowly his or her body breaks down treatment. Each person’s PK profile is different, and treatment can be personalized to your profile.5

About ADVATE

For adults and children with hemophilia A, ADVATE temporarily replaces the clotting factor VIII that's missing or low in the blood.6,7 In 2003, ADVATE became the first recombinant factor VIII treatment free of blood-based additives.7,8

What does recombinant factor VIII mean?

Today, clotting factor VIII concentrates can be made without human plasma. These types of infusions are called recombinant clotting factors. Recombinant factor VIII was one of the first treatments approved for hemophilia that didn't pose the threat of transmitting a blood-borne virus.6

Flexibility to plan your peaks for your lifestyle

ADVATE is infused every 2 or 3 days (2 to 4 times per week) for prophylaxis, depending on your response and what you and your healthcare team decide is right for you. Depending on your lifestyle and dosing schedule, you may want a treatment plan with multiple peaks every week.

An image showing an example of a patient's schedule with ADVATE infusions multiple times a week. Depending on your lifestyle and dosing schedule, you may want a treatment plan with multiple peaks every week.

Hypothetical scenario, talk to your doctor before participating in any physical activity.

A legacy of real patient experience

over
20
years

Over 20 years of treatment experience in the real world.7

over
46
billion

ADVATE is a global leader in factor VIII treatment, with over 46 billion International Units distributed globally.‡8

As of August 2024.

#1
for on-demand use

ADVATE is the most prescribed factor VIII product used for breakthrough bleeds in patients on non-factor therapy, and for patients receiving on-demand treatment only.§

§Based on market reporting of units sold from October 2019 to September 2024.

3
indications

ADVATE is indicated for prophylaxis, on-demand, and surgical use to help prevent bleeding episodes in children and adults.7

Committed to advancing hemophilia A care

Since introducing the first recombinant factor VIII treatment, Takeda has made advancements in dosing options, reconstitution with BAXJECT III®, and the introduction of myPKFiT® for personalized treatment.7,8

2003
ADVATE: First recombinant factor VIII (rFVIII) made without added human or animal proteins.7,8
2006
BAXJECT II® needleless transfer device.8
2007
First rFVIII 3000-IU single-vial dose.8
2010
First and only rFVIII 1700-IU single-vial dose.8
2011
First and only rFVIII with physical health–related quality-of-life results in the Prescribing Information.7
2012
First and only rFVIII 4000-IU single-vial dose and 2-mL diluent option (250 IU, 375 IU, 500 IU, 750 IU, 1000 IU, 1500 IU, and 1700 IU).7,8
2014
ADVATE with BAXJECT III® reconstitution system.8
2018
myPKFiT for ADVATE receives approval from the FDA for patients 16 and older.8

Explore ADVATE
safety information

Learn about health-related
quality-of-life data