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emtricitabine + tenofovir disoproxil fumarate + T101

Development stage
Unknown
Lead developer
Tasly Biopharmaceuticals
Modality
Small Molecules, Vaccines & Immunotherapeutics
Administration
Intramuscular, Oral
01

Overview

This combination therapy is being evaluated for the treatment of chronic hepatitis B (CHB) and consists of the therapeutic vaccine **T101** administered alongside the nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) **emtricitabine** and **tenofovir disoproxil fumarate**. T101 is a recombinant adenovirus serotype 5 (Ad5) viral vector vaccine developed by Tasly Tianjin Biopharmaceutical, utilizing Transgene's TG1050 technology platform. It is engineered to express three essential hepatitis B virus (HBV) antigens—polymerase, core, and surface antigens—to stimulate a robust, multi-specific T-cell response aimed at achieving a functional cure. Emtricitabine and tenofovir disoproxil fumarate (often administered as the fixed-dose combination Truvada) serve as potent antiviral agents that inhibit HBV DNA polymerase, thereby suppressing viral replication. The combination strategy aims to reduce the viral load while simultaneously re-educating the host immune system to recognize and clear HBV-infected hepatocytes.

Brand names
Truvada
Other names
Therapeutic Hepatitis B Adenovirus Injection + emtricitabine + tenofovir disoproxil fumarateT101 Combined With Nucleoside AnaloguesT-101 Combined With Nucleoside AnaloguesT 101 Combined With Nucleoside Analogues
02

Targets

HBV Pol (Hepatitis B virus polymerase)HBc (Hepatitis B virus core protein)HBsAg (Hepatitis B surface antigen)

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