Regeneron is conducting a study enrolling male participants with haemophilia B

You may help progress the understanding of haemophilia B

Honey-B aims to evaluate disease characteristics in people with haemophilia B who are receiving FIX prophylaxis.


This website provides information about a study, Honey-B, for boys and men with haemophilia B. Haemophilia B is a rare genetic disease characterised by abnormally low amounts of functional Factor IX (factor nine) protein. Factor IX (FIX) is a protein made naturally in the body and helps the blood to form clots to stop bleeding. FIX is expressed by a gene located on the X chromosome. Men have only one X chromosome, while women have two X chromosomes. Because of this, severe haemophilia more often affects men as they do not have a second copy of the gene. People with moderate and severe haemophilia B have spontaneous bleeding inside the body, pain and heavy bleeding after a cut or injury.

This disease affects about 4 in every 100,000 men worldwide, according to the World Federation of Haemophilia (WFH).


Studies help doctors to better understand how a disease affects patients and how a potential treatment for the disease works in the body. This study plays an important role in increasing doctors’ understanding of haemophilia B, which may help other people with haemophilia B in the future.

Learn more about Honey-B and see if it may be an option for you or someone you know.

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