Emerging drugs for hepatitis D.
Chronic hepatitis delta
bulevirtide, lonafarnib
nucleic acid polymers
pegylated interferon alfa
pegylated interferon lambda
treatment
Journal
Expert opinion on emerging drugs
ISSN: 1744-7623
Titre abrégé: Expert Opin Emerg Drugs
Pays: England
ID NLM: 101135662
Informations de publication
Date de publication:
12 2023
12 2023
Historique:
medline:
29
6
2023
pubmed:
25
4
2023
entrez:
25
04
2023
Statut:
ppublish
Résumé
Chronic hepatitis delta (CHD) is the most severe form of chronic viral hepatitis. Until recently, its treatment consisted of pegylated interferon alfa (pegIFN) use. Current and new drugs for treating CHD. Virus entry inhibitor bulevirtide has received conditional approval by the European Medicines Agency. Prenylation inhibitor lonafarnib and pegIFN lambda are in phase 3 and nucleic acid polymers in phase 2 of drug development. Bulevirtide appears to be safe. Its antiviral efficacy increases with treatment duration. Combining bulevirtide with pegIFN has the highest antiviral efficacy short-term. The prenylation inhibitor lonafarnib prevents hepatitis D virus assembly. It is associated with dose-dependent gastrointestinal toxicity and is better used with ritonavir which increases liver lonafarnib concentrations. Lonafarnib also possesses immune modulatory properties which explains some post-treatment beneficial flare cases. Combining lonafarnib/ritonavir with pegIFN has superior antiviral efficacy. Nucleic acid polymers are amphipathic oligonucleotides whose effect appears to be a consequence of phosphorothioate modification of internucleotide linkages. These compounds led to HBsAg clearance in a sizable proportion of patients. PegIFN lambda is associated with less IFN typical side effects. In a phase 2 study it led to 6 months off treatment viral response in one third of patients.
Identifiants
pubmed: 37096555
doi: 10.1080/14728214.2023.2205639
doi:
Substances chimiques
Antiviral Agents
0
lonafarnib
IOW153004F
Nucleic Acids
0
Polyethylene Glycols
3WJQ0SDW1A
Polymers
0
Ritonavir
O3J8G9O825
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM