Bulevirtide
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| Trade names | Hepcludex |
| Other names | MyrB, Myrcludex-B[1] |
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| Routes of administration | Subcutaneous |
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| Formula | C248H355N65O72 |
| Molar mass | 5398.951 g·mol−1 |
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Bulevirtide, sold under the brand name Hepcludex, is an antiviral medication for the treatment of chronic hepatitis D (in the presence of hepatitis B).[6]
The most common side effects include raised levels of bile salts in the blood and reactions at the site of injection.[6]
Bulevirtide works by attaching to and blocking a receptor (target) through which the hepatitis delta and hepatitis B viruses enter liver cells.[6] By blocking the entry of the virus into the cells, it limits the ability of HDV to replicate and its effects in the body, reducing symptoms of the disease.[6]
Bulevirtide was approved for medical use in the European Union in July 2020.[6]
- ^ Deterding K, Wedemeyer H (2019). "Beyond Pegylated Interferon-Alpha: New Treatments for Hepatitis Delta". AIDS Reviews. 21 (3): 126–134. doi:10.24875/AIDSRev.19000080. PMID 31532397. S2CID 202674681.
- ^ a b "Hepcludex (bulevirtide acetate)". Therapeutic Goods Administration (TGA). 12 August 2024. Retrieved 12 October 2024.
- ^ "Therapeutic Goods (Poisons Standard—June 2024) Instrument 2024". Federal Register of Legislation. 30 May 2024. Retrieved 10 June 2024.
- ^ "Hepcludex (Gilead Sciences Pty Ltd)". Therapeutic Goods Administration (TGA). 13 September 2024. Retrieved 15 September 2024.
- ^ "Hepcludex 2 mg powder for solution for injection - Summary of Product Characteristics (SmPC)". (emc). 30 March 2022. Retrieved 1 July 2022.
- ^ a b c d e f Cite error: The named reference
Hepcludex EPARwas invoked but never defined (see the help page). - ^ "Hepcludex Product information". Union Register of medicinal products. Retrieved 3 March 2023.