Drug intelligence / Profile preview

interferon alpha + nucleoside analogue

Development stage
Unknown
Lead developer
Sun Yat-sen University
Modality
Cytokines & Interferons → Recombinant Proteins and Enzymes, Small Molecules
Administration
Subcutaneous, Oral
01

Overview

interferon alpha + nucleoside analogue is a combination therapy regimen investigated by Sun Yat-sen University for the treatment of HBeAg-positive chronic hepatitis B. The treatment strategy involves an initial 12-week course of interferon alpha (IFN-α), followed by the addition of a nucleoside analogue (specifically lamivudine in the primary study protocol) for patients who do not achieve an early virological response (HBV DNA < 1000 copies/ml) or remain HBeAg positive at week 12. Interferon alpha functions as an immunomodulator and antiviral agent by activating the JAK-STAT signaling pathway through the IFNAR1 and IFNAR2 receptors, leading to the induction of interferon-stimulated genes that inhibit viral protein synthesis and assembly. The nucleoside analogue component acts as a competitive inhibitor of the Hepatitis B virus (HBV) DNA polymerase, causing premature chain termination of the viral DNA during reverse transcription. This combination approach aims to maximize viral suppression and increase the likelihood of HBeAg seroconversion compared to interferon monotherapy.

Other names
interferon alpha + lamivudineIFN-alpha plus NAinterferon alpha plus nucleoside analogue
02

Targets

IFNAR (Immune system modulation via type I interferon receptor)HBV Pol (Hepatitis B virus polymerase)

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