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REP 2165-Mg + peginterferon alfa-2a + tenofovir disoproxil fumarate
- Development stage
- Discontinued
- Lead developer
- Replicor
- Modality
- Small Molecules, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Recombinant Proteins and Enzymes, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics
- Administration
- Intravenous, Subcutaneous, Oral
01
Overview
This is a **combination therapy** comprising **REP 2165-Mg** (a nucleic acid polymer or NAP, magnesium chelate formulation), **peginterferon alfa-2a** (a pegylated recombinant interferon, immune modulator), and **tenofovir disoproxil fumarate** (a nucleotide reverse transcriptase inhibitor). The combination has been investigated in **clinical trials for the treatment of chronic hepatitis B** (HBV), particularly in HBeAg-negative patients. REP 2165-Mg acts as a hepatitis B virus replication inhibitor by blocking secretion of hepatitis B surface antigen (HBsAg) from infected hepatocytes, aiming to enhance immune restoration. Peginterferon alfa-2a binds to type I interferon receptors, activating the JAK/STAT pathway and inducing the innate antiviral response. Tenofovir disoproxil fumarate inhibits HBV DNA polymerase, blocking reverse transcription and viral replication. The **combination is designed to reduce HBsAg levels, suppress HBV DNA, and promote seroconversion, potentially leading to a functional cure.** REP 2165-Mg was developed by Replicor; the formulation uses branded products Pegasys (peginterferon alfa-2a, Roche) and Viread (tenofovir disoproxil fumarate, Gilead).
- Other names
- REP 2165 magnesium chelateREP2165 magnesium chelateREP-2165 magnesium chelatepegylated interferon alfa-2aTDF
02
Targets
IFNAR (Immune system modulation via type I interferon receptor)HBV Pol (Hepatitis B virus polymerase)
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