Nitisinone 2mg capsules
Requires a prescription from a doctor or prescriber
Nitisinone is a synthetic reversible inhibitor of 4-hydroxyphenylpyruvate dioxygenase.
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Yellow Card reports
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Suspected adverse reactions reported for Nitisinone
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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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Suspected adverse reactions reported for Nitisinone
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3 branded products available
MHRA licensed products
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Orfadin 2mg capsules
Nitisinone 2mg capsules
WHO defined daily dose (DDD)
20 mg
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
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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
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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. 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: 17 · Randomised trials: 3 · 2005–2026
Showing the 50 most relevant studies, sorted by most relevant.
Wendy J. Introne, Monique B. Perry, James Troendle, et al.
Molecular Genetics and Metabolism, 2011
- Alkaptonuria
- Cyclohexanones
- Homogentisic Acid
L. Ranganath, Eftychia Eirini Psarelli, Jean-Baptiste Arnoux, et al.
The Lancet Diabetes & Endocrinology, 2020
- Alkaptonuria
- Cyclohexanones
- Enzyme Inhibitors
Flávia Diniz Mayrink, Gilson Pires Dorneles, Igor Martins da Silva, et al.
Molecular Genetics and Metabolism, 2025
- Alkaptonuria
- Cyclohexanones
- Nitrobenzoates
Endocrine Practice, 2025
Julia Geppert, Chris Stinton, Karoline Freeman, et al.
Orphanet Journal of Rare Diseases, 2017
- Cyclohexanones
- Nitrobenzoates
- Neonatal Screening
Martin Nelwan
African Journal of Biological Sciences, 2021
C. Stinton, J. Geppert, K. Freeman, et al.
Journal of Epidemiology & Community Health, 2017
Bruce C, Meenamkuzhy-Hariharan P, Hussain S, et al.
2025
Background and aim Alkaptonuria (AKU) is a rare metabolic disorder characterised by the accumulation of homogentisic acid (HGA). Deposition of HGA in the aortic valve leading to progressive aortic stenosis is a serious complication. Nitisinone has been shown to improve morbidity and slow disease progression in AKU, but the effects of this treatment on aortic stenosis progression have not yet been described. The objective of this study was to evaluate whether treatment with nitisinone attenuated the progression of aortic stenosis, as assessed by peak trans-aortic valve pressure (Pmax), in patients with AKU. This post-hoc analysis used longitudinal echocardiographic data from the Suitability of Nitisinone in Alkaptonuria (SONIA) 2, a four-year multicenter randomised controlled trial, to examine aortic stenosis disease progression. Methods Data were obtained from echocardiograms performed on 138 patients over 48 months of follow-up. A linear mixed-effects regression model was used to ascertain the difference in the maximal trans-aortic valve pressure gradient (Pmax) at baseline and 48 months between the treatment and control groups, adjusting for baseline Pmax and other covariates. Results At baseline, 18/138 patients (13.0%) had aortic stenosis of varying degrees of severity, and 25/138 (18.1%) had aortic sclerosis. The difference in Pmax between the control (N=69) and treatment (N=69) groups at baseline was 0.063 mmHg [95% CI: -0.054 mmHg to 0.18 mmHg) and did not reach statistical significance (p=0.23). At the end of the four-year treatment period, the difference in Pmax was 0.10 mmHg (95% CI: -0.0007 mmHg to 0.20 mmHg) (p = 0.05), representing a modest but statistically significant between-group treatment effect. Conclusion Nitisinone may attenuate the progression of aortic stenosis in patients with AKU. Given the small absolute effect size and post-hoc nature of the analysis, these findings should be interpreted as exploratory and hypothesis-generating rather than clinically definitive. Additional research is needed to determine whether nitisinone produces clinically meaningful outcomes for aortic stenosis in this population.
Abstract licence: CC BY
Pim Suwannarat, Kevin O’Brien, Monique B. Perry, et al.
Metabolism, 2005
- Alkaptonuria
- Cyclohexanones
- Dietary Proteins
L. Ranganath, Anna M. Milan, Andrew T. Hughes, et al.
Annals of the Rheumatic Diseases, 2014
- Alkaptonuria
- Cyclohexanones
- Enzyme Inhibitors
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
None known
Half-life
Not available
Mechanism
Nitisinone is a competitive inhibitor of 4-hydroxyphenyl-pyruvate dioxygenase, a…
Food interactions
3 warnings
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
Protein binding
95%
[L53258]
Volume of distribution
[L53258]
Elimination
[L53258]
Clearance
0.003 L/h
[L53258]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L53253]
Under the name HARLIKU, nitisinone is indicated for the reduction of urine homogentisic acid (HGA) in adult patients with
alkaptonuria (AKU).
[L53258]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L53258]
[L53258]
[L53258]
[L53258]
Proteins and enzymes this drug interacts with in the body
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC A16AX04
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)
Nitisinone
Additional database identifiers
Drugs Product Database (DPD)
22811
ChemSpider
103195
BindingDB
50088804
ZINC
ZINC000100014475
HUGO Gene Nomenclature Committee (HGNC)
HGNC:5147
GenAtlas
HPD
GeneCards
HPD
GenBank Gene Database
U29895
GenBank Protein Database
3860238
UniProt Accession
HPPD_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q3877355), 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.