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All Oral Interferon-free Direct-acting Antivirals as Combination Therapies to Cure Hepatitis C
Imran Shahid1,2, Munjed M Ibrahim3
1Department of Pharmacology and Toxicology, College of Pharmacy, Umm Al Qura University, Al-Abidiyah, Makkah, P.O Box. 13578, Postal code 21955, Saudi Arabia.
Insights
Direct-acting antivirals (DAAs) offer a breakthrough for chronic hepatitis C (CHC) treatment, achieving high cure rates. Interferon-free regimens are revolutionizing care and advancing global hepatitis C virus (HCV) elimination goals.
Area of Science:
- Hepatology
- Virology
- Infectious Diseases
Background:
- Chronic hepatitis C virus (HCV) infection presents a significant global health challenge with historically poor treatment rates.
- Traditional dual-therapy with pegylated interferon (PEG-IFN) and ribavirin (RBV) demonstrated suboptimal treatment completion in real-world settings.
Purpose of the Study:
- To comprehensively review the evolution and efficacy of interferon-free direct-acting antiviral (DAA) regimens for treating chronic hepatitis C (CHC).
- To highlight the advancements in HCV therapeutics and their impact on achieving global HCV elimination targets.
Main Methods:
- Review of current literature on direct-acting antiviral (DAA) therapies for hepatitis C virus (HCV).
- Analysis of clinical efficacy, sustained virologic response (SVR) rates, resistance profiles, and adverse events associated with various DAA regimens.
- Evaluation of the shift from interferon-based therapies to oral, interferon-free DAA treatment paradigms.
Main Results:
- Direct-acting antivirals (DAAs), including fixed-dose combinations, show high clinical efficacy across different HCV genotypes and patient populations.
- Novel pan-genotypic anti-HCV regimens achieve very high sustained virologic response (SVR) rates with a high barrier to drug resistance.
- Interferon-free DAAs exhibit a low frequency of adverse events and fewer drug-drug interactions compared to older therapies.
Conclusions:
- Interferon-free DAAs have revolutionized hepatitis C virus (HCV) treatment, shifting the paradigm towards highly effective oral therapies.
- These advancements provide a strategic approach to reduce HCV-related morbidity and mortality, supporting global elimination efforts.
- The development of novel DAA regimens is crucial for achieving the worldwide goal of HCV elimination in the near future.
Abstract:
Chronic hepatitis C (CHC) virus infection and associated hepatic diseases are still challenging, and the disease burden remains significant around the world. Overall treatment rates for the chronically infected patients have been "dismally poor" and that treatment completion of dual-therapy- pegylated interferon (PEG-IFN) and ribavirin (RBV) is suboptimal in the real-world clinical settings. The approval of first, second and next-generation direct-acting antivirals (DAAs) represents a major breakthrough in hepatitis C virus (HCV) therapeutics to treat CHC infected individuals. Such therapeutic regimens in a fixed dose combination (FDC) or along with RBV have proven their clinical efficacy against different HCV genotypes, and harder-to-treat special populations. We continue to see the development of novel pan-genotypic anti-HCV regimens with very high sustained virologic response (SVR; undetectable viral load at week 12 or at the end of therapy) rates, high barrier to drug resistance, low frequency of adverse events, and fewer drug-drug interactions as compared to some older RBV based triple DAA therapies. Oral interferon-free DAAs seem highly successful strategic treatment approaches against hepatitis C and impulse health policy makers to establish the treatment priorties and policies to reduce the rate of hepatitis C-related morbidity and mortality. This review article comprehensively overviews interferon-free anti-HCV regimens, which have totally shifted the treatment paradigms for hepatitis C with some additional benefits to galvanize our efforts to achieve the global goal of HCV elimination in near future.
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