Drug intelligence / Profile preview

ravidasvir + sofosbuvir + ribavirin

Development stage
Unknown
Lead developer
Drugs for Neglected Diseases initiative
Modality
Small Molecules
Administration
Oral
01

Overview

A fixed-dose combination of **ravidasvir**, **sofosbuvir**, and **ribavirin** used for the treatment of chronic hepatitis C virus (HCV) infection, particularly genotype 4, and sometimes genotype 1 and 3. Ravidasvir is a pangenotypic non-structural protein 5A (NS5A) inhibitor; sofosbuvir is a nucleotide analogue inhibitor of NS5B polymerase; ribavirin is a guanosine analogue with broad antiviral activity but is not effective alone and must be combined with other agents. The regimen is used in both treatment-naïve and treatment-experienced adult patients, with or without compensated cirrhosis. Ribavirin is especially added for patients with cirrhosis or those with difficult-to-cure genotypes. The mechanism involves inhibition of HCV replication: ravidasvir blocks NS5A-mediated RNA replication/assembly; sofosbuvir inhibits NS5B polymerase-dependent replication; ribavirin enhances viral mutagenesis and immune modulation. The combination has shown high sustained virologic response rates (SVR12 95–97%) and is well tolerated, though ribavirin can cause hematological side effects. Developed for affordability to support public health efforts in resource-limited regions, notably Egypt, Malaysia, and Thailand[1][2][4][5][6].

02

Targets

NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))

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