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EMA Product

Hepcludex

Product approved by European Medicines Agency (EU)

Basic Information

Hepcludex

Regulatory Information

EMEA/H/C/004854

Authorised

July 31, 2020

14

February 4, 2025

Company Information

Ireland

Carrigtohill County Cork T45 DP77

GILEAD SCIENCES IRELAND UC

Drug Classification

Orphan MedicineAdditional Monitoring

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Hepcludex is indicated for the treatment of chronic hepatitis delta virus (HDV) infection in plasma (or serum) HDV-RNA positive adult and paediatric patients 3 years of age and older weighing at least 10 kg with compensated liver disease.

Overview Summary

Hepcludex is an antiviral medicine used to treat chronic (long-term) hepatitis delta virus (HDV) infection in adults and children from 3 years of age and weighing at least 10 kg who have compensated liver disease (when the liver is damaged but is still able to work). It is used when the presence of HDV RNA (genetic material) has been confirmed by blood tests. HDV is an 'incomplete' virus, because it cannot replicate in cells without the help of another virus, the hepatitis B virus. Because of this, patients infected with the virus always also have hepatitis B. HDV infection is rare, and Hepcludex was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 19 June 2015. Further information on the orphan designation can be found on the EMA [website](http://www.ema.europa.eu/medicines/human/orphan-designations/eu3151500). Hepcludex contains the active substance bulevirtide.

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