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©The Author(s) 2025.
World J Hepatol. Apr 27, 2025; 17(4): 105797
Published online Apr 27, 2025. doi: 10.4254/wjh.v17.i4.105797
Published online Apr 27, 2025. doi: 10.4254/wjh.v17.i4.105797
Table 1 Current available drugs for the treatment of chronic hepatitis B
Types of drugs | Name | Antiviral mechanism | Limitations/comments |
Immunomodulators | IFN-2α and PEG-IFN-2α | Inhibit HBV replication Activate antiviral immune responses | Poor tolerability; Anti-PEG antibody mediated immune clearance[4] |
Nucleoside analogue | ETV | HBV DNA polymerase inhibitor | High potency and low resistance |
Nucleotide analogue | TDF | HBV DNA polymerase inhibitor | Potent, but with kidney and bone toxicity concern in long-term use |
Nucleotide analogue | TAF | HBV DNA polymerase inhibitor | TDF analog with improved renal and bone safety profiles |
Nucleotide analogue | ADV | HBV DNA polymerase inhibitor | Less potent, nephrotoxicity |
Nucleoside analogue | 3TC | HBV DNA polymerase inhibitor | Less potent, high rate of resistance |
Nucleoside analogue | LdT | HBV DNA polymerase inhibitor | High rate of resistance |
- Citation: Liu T, Wang H, Zhao Y, Wang YX, Xing X, Gao P. Drug development for chronic hepatitis B functional cure: Recent progress. World J Hepatol 2025; 17(4): 105797
- URL: https://www.wjgnet.com/1948-5182/full/v17/i4/105797.htm
- DOI: https://dx.doi.org/10.4254/wjh.v17.i4.105797