Drug intelligence / Profile preview

entecavir + tenofovir alafenamide + tenofovir disoproxil fumarate + tenofovir amibufenamide + peginterferon alfa

Development stage
Unknown
Lead developer
Huashan Hospital
Modality
Cytokines & Interferons → Recombinant Proteins and Enzymes, Small Molecules
Administration
Oral, Subcutaneous
01

Overview

This combination therapeutic regimen consists of four nucleos(t)ide analogues (entecavir, tenofovir alafenamide, tenofovir disoproxil fumarate, and tenofovir amibufenamide) and peginterferon alfa. It is being evaluated in the REASON study, a multicenter observational study led by Huashan Hospital in China, for the treatment of chronic hepatitis B (CHB). The regimen combines potent viral suppression via multiple polymerase inhibitors with the immunomodulatory effects of interferon to optimize treatment outcomes, particularly in patients who are treatment-naive or have had partial responses to first-line therapies. Tenofovir amibufenamide (TMF) is a novel tenofovir prodrug developed in China by Hansoh Pharma that offers improved plasma stability and targeted delivery to the liver compared to older tenofovir formulations.

Other names
entecavir + tenofovir alafenamide + tenofovir disoproxil fumarate + TMF + interferonETV + TAF + TDF + TMF + IFN
02

Targets

IFNAR2 (Interferon alpha/beta receptor subunit 2)IFNAR1 (Interferon alpha/beta receptor 1)HBV Pol (Hepatitis B virus polymerase)

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