Boceprevir 200mg capsules
Boceprevir is a direct acting antiviral medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV).
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Boceprevir
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Report a side effect
Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Boceprevir
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Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
WHO defined daily dose (DDD)
2.4 gram
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(6)
Elbasvir–grazoprevir for treating chronic hepatitis C (TA413)
Peginterferon alfa and ribavirin for treating chronic hepatitis C in children and young people (TA300)
Sofosbuvir for treating chronic hepatitis C (TA330)
Sofosbuvir–velpatasvir for treating chronic hepatitis C (TA430)
Ombitasvir–paritaprevir–ritonavir with or without dasabuvir for treating chronic hepatitis C (TA365)
Ledipasvir–sofosbuvir for treating chronic hepatitis C (TA363)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 14 · Randomised trials: 4 · 2008–2024
Showing the 50 most relevant studies, sorted by most relevant.
P. Kwo, E. Lawitz, J. McCone, et al.
Lancet, 2010
- Interferon alpha-2
- Viral Proteases
- Antiviral Agents
M. Sulkowski, S. Pol, J. Mallolas, et al.
The Lancet. Infectious diseases, 2013
- Interferon alpha-2
- Antiviral Agents
- Genotype
Chunlong Ma, M. Sacco, Brett L. Hurst, et al.
Cell Research, 2020
- A549 Cells
- Betacoronavirus
- COVID-19
Lifeng Fu, Fei Ye, Yong Feng, et al.
Nature Communications, 2020
- Betacoronavirus
- COVID-19
- SARS-CoV-2
H. Wedemeyer, X. Forns, C. Hézode, et al.
PLoS ONE, 2016
J. Diels (6377402), S. Gavart (8414295), E. Jones (3511811), et al.
2020
Nicola Coppola, Mariantonietta Pisaturo, Caterina Sagnelli, et al.
PLoS ONE, 2014
- Interferon alpha-2
- Antiviral Agents
- Clinical Trials as Topic
María del Carmen Manzano-Robleda, Victoria Ornelas-Arroyo, Tonatiuh Barrientos‐Gutiérrez, et al.
Annals of Hepatology, 2015
- Interferon alpha-2
- Antiviral Agents
- Oligopeptides
Mugdha Sitole, Matthew J. Silva, Linda M. Spooner, et al.
Clinical Therapeutics, 2013
- Oligopeptides
- Polyethylene Glycols
- Proline
J. Vierling, S. Zeuzem, F. Poordad, et al.
Journal of hepatology, 2014
- Antiviral Agents
- Liver Cirrhosis
- Polyethylene Glycols
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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
2 found
Half-life
3.4 hours
Mechanism
Boceprevir is a NS3/4a protease inhibitor used to inhibit viral HCV replication [FDA Label].
Food interactions
1 warning
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
2 hours
Half-life
3.4 hours
Protein binding
75%
Volume of distribution
Metabolism
Elimination
79%
Clearance
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
In a joint recommendation published in 2016, the American Association for the Study of Liver Diseases (AASLD) and the Infectious Diseases Society of America (IDSA) do not reccomend Boceprevir in combination with DB00811, DB00008, and DB00022 as first line therapy for Hepatitis C [A19593]. Boceprevir, DB00811, DB00008, and DB00022 are used with the intent to cure, or achieve a sustained virologic response (SVR), after 48 weeks of daily therapy. SVR and eradication of HCV infection is associated with significant long-term health benefits including reduced liver-related damage, improved quality of life, reduced incidence of Hepatocellular Carcinoma, and reduced all-cause mortality [A19626].
Boceprevir is available as a fixed dose product (tradename Victrelis) used for the treatment of chronic Hepatitis C. Approved in May 2011 by the FDA, Victrelis is indicated for the treatment of HCV genotype 1 in combination with DB00811, DB00008, and DB00022 [FDA Label]. Victrelis is no longer widely used as interferon-free therapies have been developed.
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 895 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
In capsule, Boceprevir consists of two diaseromers in a 1:1 ratio. In plasma this ratio changes to 2:1 favoring the active diastereomer.
Enzymes involved in drug metabolism — important for understanding drug interactions
Proteins that transport this drug across cell membranes
PMID:2897240 PMID:35970996 PMID:8898203 PMID:9038218 PMID:35507548
Catalyzes the flop of phospholipids from the cytoplasmic to the exoplasmic leaflet of the apical membrane. Participates mainly to the flop of phosphatidylcholine, phosphatidylethanolamine, beta-D-glucosylceramides and sphingomyelins .
PMID:8898203
Energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells PMID:2897240 PMID:35970996 PMID:9038218
ATC J05AP03
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Boceprevir
Additional database identifiers
Drugs Product Database (DPD)
20878
ChemSpider
8499830
BindingDB
12311
PDB
HU5
UniProt Accession
B0B3C9_9HEPC
GenBank Gene Database
M62321
UniProt Accession
POLG_HCV1
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2638
GenAtlas
CYP3A5
GeneCards
CYP3A5
GenBank Gene Database
J04813
GenBank Protein Database
181346
Guide to Pharmacology
1338
UniProt Accession
CP3A5_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:40
GenAtlas
ABCB1
GeneCards
ABCB1
GenBank Gene Database
M14758
GenBank Protein Database
307180
Guide to Pharmacology
768
UniProt Accession
MDR1_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q410551), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.