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Recent Advancement of Direct-acting Antiviral Agents (DAAs) in Hepatitis C Therapy
1Department of Chemistry, School of Science, RK University, Rajkot-360020, Gujarat, India.
Insights
Direct-acting antiviral agents (DAAs) offer effective, interferon-free treatment for chronic Hepatitis C virus (HCV) infection. This review covers clinical trial results of new DAAs and approved combinations, including their advancements and side effects.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Chronic Hepatitis C virus (HCV) infection affects 170-200 million globally, posing risks for liver cirrhosis and cancer.
- Complete HCV eradication is a primary goal of antiviral research.
- First-generation protease inhibitors (boceprevir, telaprevir) were approved in 2011.
Purpose of the Study:
- To review clinical trial results of direct-acting antiviral agents (DAAs) for Hepatitis C.
- To discuss approved DAA combinations and their efficacy.
- To cover the latest advancements and side effects of DAA therapy.
Main Methods:
- Review of clinical trial data for various DAAs.
- Analysis of approved combination therapies.
- Discussion of drug classes: NS3/4A protease inhibitors, NS5A inhibitors, and NS5B inhibitors.
Main Results:
- New DAAs demonstrate increased efficacy, safety, and tolerability.
- Interferon-free oral therapies are now standard for chronic HCV and cirrhosis.
- Several DAA medications (Sovaldi®, Harvoni®, Viekira Pak®, Epclusa®, Zepatier®) have received FDA approval.
Conclusions:
- DAAs represent a significant advancement in Hepatitis C treatment.
- Interferon-free regimens have transformed HCV management.
- Ongoing research focuses on optimizing DAA therapy and managing potential side effects.
Abstract:
Hepatitis C virus (HCV) infection is a major health problem worldwide. Approximately, 170-200 million individuals are chronically infected worldwide and a quarter of these patients are at increased risk of developing liver cirrhosis, hepatocellular carcinoma and even liver failure. A complete eradication of the virus is one of the most important treatment goals for antiviral research. In 2011, the first-generation protease inhibitors boceprevir (BOC) telaprevir (TVR) were approved by FDA as the direct-acting antiviral agents. A number of promising new direct-acting antiviral agents (DAAs) have been developed in the past few years. Due to their increased efficacy, safety, and tolerability, interferon-free oral therapies with DAAs are in use for patients with chronic HCV and cirrhosis patients. In this review, we will discuss the results of clinical trials of several DAAs and the approved combinations, including NS3/4A protease inhibitors, NS5A inhibitors, and NS5B inhibitors. A number of drugs, including Sovaldi®, Harvoni® Viekira Pak®, Epclusa®, Zepatier® have been approved by FDA in the past two-three years. The latest advancement of DAA therapy and related side effects due to the therapy are also discussed.
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