Elbasvir 50mg / Grazoprevir 100mg tablets
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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2 branded products available
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View all licensed products for Elbasvir + Grazoprevir on the MHRA register
Zepatier 50mg/100mg tablets
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 13 · Randomised trials: 18 · 2015–2026
Showing the 50 most relevant studies, sorted by most relevant.
G. Dore, F. Altice, A. Litwin, et al.
Annals of internal medicine, 2016
- Opiate Substitution Treatment
- Hepatitis C, Chronic
- Opioid-Related Disorders
Jafari M, Mehdizadeh P, Teymourzadeh E, et al.
2025
OBJECTIVES: Direct-acting antivirals (DAAs) have revolutionized hepatitis C (HCV) treatment, yet their high cost necessitates rigorous economic evaluation. Glecaprevir/Pibrentasvir (GLE/PIB) and Grazoprevir/Elbasvir (GZR/EBR) are two key, highly effective DAA regimens, but their comparative cost-effectiveness across different healthcare settings remains unclear. This study aims to systematically review and qualitatively synthesize the economic evidence for GLE/PIB and GZR/EBR, comparing them with each other and other relevant HCV treatments. METHODS: A systematic review was conducted by searching PubMed, Scopus, Embase, Science Direct, and the Cochrane Library for full economic evaluation studies published up to September 2025. The quality of included studies was assessed using the CHEERS checklist. Due to significant heterogeneity in study contexts, populations, and methodologies, a qualitative narrative synthesis was performed, and quantitative pooling of economic outcomes was avoided. RESULTS: A total of 20 economic evaluation studies were included. Both GLE/PIB and GZR/EBR were consistently found to be cost-effective or dominant strategies when compared to older interferon-based therapies. However, the five head-to-head studies comparing GLE/PIB and GZR/EBR yielded conflicting results: GLE/PIB was the economically preferred option in settings like Japan and Brazil, whereas GZR/EBR was favored in analyses from China and Hong Kong. This variability appears to be primarily driven by differences in local drug acquisition prices. CONCLUSION: Neither GLE/PIB nor GZR/EBR can be considered universally more cost-effective than the other. Both regimens represent valuable advancements over previous standards of care, but the optimal economic choice between them is highly context-dependent. These findings underscore the necessity of using local, setting-specific economic evaluations to inform clinical guidelines and reimbursement policies.
Abstract licence: CC BY-NC-ND
Hussien Ahmed, Abdelrahman Ibrahim Abushouk, Amr Menshawy, et al.
Annals of Hepatology, 2018
E. Lawitz, F. Poordad, J. Gutierrez, et al.
Hepatology, 2017
- Hepacivirus
- Hepatitis C
- Hepatitis C, Chronic
Jinyu Liu, Min Guo, Lei Ke, et al.
Frontiers in Public Health, 2022
- Hepatitis C, Chronic
- Hepacivirus
- Amides
ObjectiveThis study aims to systematically review recent economic evaluations of elbasvir/grazoprevir (EBR/GZR) for chronic hepatitis C (CHC), to critically appraise the reporting quality and to summarize the results.MethodsA literature search was undertaken using Medline, Embase, the Cochrane Library, EconLit, China National Knowledge Infrastructure, Wanfang Data, and Chongqing VIP to identify original articles containing economic evaluations of EBR/GZR for CHC published between 1 January 2000 and 31 December 2020. The Consolidated Health Economic Evaluation Reporting Standards statement was used to assess the quality of reporting of the articles.ResultsOf 93 articles identified, 13 studies fulfilled the inclusion criteria. These studies were conducted in 4 countries, and 8 active interventions were assessed. The target population was patients infected with CHC genotype 1 infection in all studies. Eight out of 13 studies that compared EBR/GZR vs. other direct antiviral agents suggested that EBR/GZR was generally more cost-effective or dominant than daclatasvir/asunaprevir (DCV/ASV), sofosbuvir/velpatasvir (SOF/VEL), ledipasvir/sofosbuvir (LDV/SOF), ombitasvir/paritaprevir/ritonavir + dasabuvir (3D) but not more cost-effective than glecaprevir/pibrentasvir (GLE/PIB). Two studies from China and one study from the USA that compared EBR/GZR vs. pegylated interferon and ribavirin (PegIFN/RBV) consistently indicated that EBR/GZR was generally more cost-effective than PegIFN/RBV. One study from Italy compared EBR/GZR with SOF + PegIFN/RBV and suggested that EBR/GZR had a lower cost and higher effectiveness. One study from France and one study from the USA confirmed that compared with non-therapy for patients with chronic kidney disease, EBR/GZR was cost-effective at commonly accepted current standards. All included studies were of good quality of reporting, with an average score of 21.9 (range 19–23).ConclusionEBR/GZR for CHC genotype 1 might be cost-effective or dominant compared with PegIFN/RBV and other direct antiviral agents (SOF/VEL, 3D, DCV/ASV, LDF/SOF) or non-therapy. However, under certain assumptions, EBR/GZR was not a cost-effective alternative for CHC patients vs. GLE/PIB.
Abstract licence: CC BY 4.0
Lei Ke (217815), Min Guo (228787), Ruxu You (2558287), et al.
2022
Lei Ke (217815), Min Guo (228787), Ruxu You (2558287), et al.
2022
Lei Ke (217815), Min Guo (228787), Ruxu You (2558287), et al.
2022
J. Sperl, G. Horváth, W. Halota, et al.
Journal of hepatology, 2016
- Hepatitis C, Chronic
- Hepacivirus
- Imidazoles
Chizoba Nwankwo, Shelby L. Corman, Elamin H. Elbasha
Journal of Infection and Public Health, 2019
- Hepacivirus
- Hepatitis C
- Amides
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.