Explore effectiveness results in LEOPOLD I

In LEOPOLD I, doctors studied annual bleed rate (ABR) with KOVALTRY®, choosing either 2x/week prophylaxis (18 people) or 3x/week prophylaxis (44 people) based on people's needs1

PEOPLE IN THE STUDY2

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ASSIGNED DOSING2

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ABR RESULTS1

PEOPLE IN THE STUDY2

Group 1 (18 people)
generally began the study with fewer bleeds and a lower percentage of target joints

ASSIGNED DOSING2

2x/week

ABR RESULTS1

1

median ABR

PEOPLE IN THE STUDY2

Group 2 (44 people)
generally began the study with more bleeds and a higher percentage of target joints

ASSIGNED DOSING2

3x/week

ABR RESULTS1

2

median ABR


When treating on demand, 87% of bleeding episodes were resolved with 2 or fewer infusions of KOVALTRY® in LEOPOLD I.1

Download the Discussion Guide to help plan a conversation with your doctor about your treatment goals

INDICATIONS

KOVALTRY® is a medicine used to replace clotting factor (Factor VIII or antihemophilic factor) that is missing in people with hemophilia A.

KOVALTRY® is used to treat and control bleeding in adults and children with hemophilia A. KOVALTRY® can reduce the number of bleeding episodes in adults and children with hemophilia A when used regularly (prophylaxis). Your healthcare provider may give you KOVALTRY® when you have surgery.

KOVALTRY® is not used to treat von Willebrand Disease.

IMPORTANT SAFETY INFORMATION

You should not use KOVALTRY® if you are allergic to rodents (like mice and hamsters) or any ingredients in KOVALTRY®.

Tell your healthcare provider if you have heart disease or are at risk for heart disease.

The common side effects of KOVALTRY® are headache, fever, and itchy rash.

Allergic reactions may occur with KOVALTRY®. Call your healthcare provider right away and stop treatment if you get tightness of the chest or throat, dizziness, decrease in blood pressure, and nausea.

Your body can also make antibodies, called "inhibitors," against KOVALTRY®, which may stop KOVALTRY® from working properly. Consult with your healthcare provider to make sure you are carefully monitored with blood tests for the development of inhibitors to Factor VIII.

Tell your healthcare provider about any side effect that bothers you or that does not go away.

Call your healthcare provider right away if bleeding is not controlled after using KOVALTRY®.

For additional important risk and use information, please see full Prescribing Information.

References: 1. KOVALTRY® [prescribing information]. Whippany, NJ: Bayer HealthCare LLC; 2016. 2. Data on file. Bayer HealthCare Pharmaceuticals, Inc; 2016.

You are encouraged to report negative side effects or quality complaints of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

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Bayer, the Bayer Cross, and KOVALTRY are registered trademarks of Bayer.

Site Last Modified 09/2017