Drug intelligence / Profile preview

BMS-650032 + peginterferon alfa-2a + ribavirin

Development stage
Unknown
Lead developer
Bristol Myers Squibb
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
Oral, Subcutaneous
01

Overview

BMS-650032 + peginterferon alfa-2a + ribavirin is a triple combination regimen developed for the treatment of chronic hepatitis C virus (HCV) infection, particularly targeting genotype 1. - BMS-650032 (asunaprevir) is an orally administered small molecule inhibitor of the HCV NS3/4A serine protease, essential for viral replication[5][9]. - Peginterferon alfa-2a is a pegylated interferon that stimulates immune response and exhibits antiviral effects[2][6][4]. - Ribavirin is a nucleoside analog with broad antiviral activity that acts synergistically with interferon-based therapies[2][4][6]. This combination has been investigated for enhanced sustained virologic response rates and overcoming resistance observed with dual therapy, especially in patients who did not previously respond to standard-of-care regimens[1][3][9].

Other names
asunaprevir + peginterferon alfa-2a + ribavirin
02

Targets

NS3/4A (Hepatitis C virus nonstructural protein 3/4A serine protease)IFNAR (Immune system modulation via type I interferon receptor)HCV RNA (Hepatitis C virus RNA)

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