4.0 Article

Beyond Pegylated Interferon-Alpha: New Treatments for Hepatitis Delta

Journal

AIDS REVIEWS
Volume 21, Issue 3, Pages 126-134

Publisher

PERMANYER PUBL
DOI: 10.24875/AIDSRev.19000080

Keywords

Hepatitis B virus/hepatitis D (delta) virus coinfection; Myrcludex B; Bulevirtide; Lonafarnib; REP-2139-Ca; Pegylated interferon-lambda

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Persistent coinfection with the hepatitis B/D viruses (HDV) represents the most severe form of viral hepatitis. Hepatitis D often leads to liver cirrhosis, hepatic decompensation, and hepatocellular carcinoma. The current treatment options are limited as only pegylated interferon-alpha (PEG-IFNce) has efficacy against HDV. However, treatment response is still unsatisfactory with 25-40% HDV RNA suppression after 1-2 years. In addition, late HDV RNA relapses have been described during long-term follow-up. Fortunately, new treatment options for patients with chronic hepatitis delta are now on the horizon. The hepatocyte entry inhibitor bulevirtide (formerly myrcludex B) and the farnesyl transferase inhibitor lonafarnib are currently explored in patients with chronic hepatitis delta in Phase 3 clinical studies. The nucleic acid inhibitor REP-2139-Ca and PEG-IFN-lambda are studied in Phase 2 trials. We here summarize data on the efficacy of these new antiviral drugs and the existing safety data on the treatment of HDV infection.

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