Calcipotriol 50micrograms/ml scalp solution
Requires a prescription from a doctor or prescriber
Calcipotriol (INN) or calcipotriene (USAN) is a sythetic derivative of calcitriol or Vitamin D.
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MHRA alerts for Calcipotriol
Safety monitoring data
Yellow Card reports
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Suspected adverse reactions reported for Calcipotriol
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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.
EudraVigilance
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Suspected adverse reactions reported for Calcipotriol
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Calcipotriol 50micrograms/ml scalp solution
Calcipotriol 50micrograms/ml scalp solution
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(1)
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
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Supply & safety information
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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
Browse tools
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: 23 · 1998–2026
Showing the 50 most relevant studies, sorted by most relevant.
T. Cunningham, M. Tabacchi, J. Eliane, et al.
Journal of Clinical Investigation, 2017
Maverakis Ramirez N, Jaeger ZJ, Lee DJ
2026
Vitiligo is a depigmentation disorder whose treatment remains a serious challenge. While it is generally accepted that topicals and phototherapy are helpful for generalized symmetric disease, randomized controlled trials (RCTs) provide the best evidence for treatment. Our objective was to identify and summarize RCTs for vitiligo from 2013 to 2023. A systematic review registered with the International Prospective Register of Systematic Reviews (PROSPERO) was performed per PRISMA guidelines. We searched CENTRAL, ClinicalTrials.gov, Embase, PubMed, and Web of Science for RCTs using keywords such as 'vitiligo' and/or 'treatment' or 'intervention.' A total of 652 studies underwent full-text review, and 151 studies met the inclusion criteria. We focused our study on RCTs using the vitiligo area scoring index (VASI) as the primary outcome measure, leading to 36 studies. We further narrowed our focus to studies that could be aggregated into the intervention categories: phototherapy and systemic combination therapy (n=10), topical and topical combination therapy (n=15), and systemic monotherapy (n=5). Treated versus control subjects showed statistically improved VASI after the following interventions were added to phototherapy: oral psoralen, oral minipulsed prednisone, implanted afamelanotide, topical ethyl vanillate, topical bimatoprost, and oral vitamins A and E. Effective topical therapies were ruxolitinib, calcipotriol and betamethasone, tacrolimus and mometasone, and microdermabrasion and tacrolimus. None of the systemic monotherapies was superior to their corresponding comparator.
Abstract licence: CC BY
Jun Yan, Shengli Chen, Juan Shi
Archives of Dermatological Research, 2023
L. Mohney, Rohan Singh, A. Grada, et al.
Journal of drugs in dermatology : JDD, 2021
A. Mahran, Alaa Ghazally, Ali S. Ali, et al.
Clinical and experimental dermatology, 2023
A. Kazeminejad, Arezo Bodaghi, Z. Hajheydari, et al.
Dermatologic Therapy, 2023
Cai L, Zhang F, Zhang G, et al.
2026
Mohammed Abu El-Hamd, Moustafa Adam El-Taieb, Faten Othman Ahmed, et al.
Journal of Skin and Stem Cell, 2025
Background: Alopecia areata (AA) is an autoimmune disease with various treatment modalities. It ranges in severity from patchy hair loss, which often resolves spontaneously, to severe, chronic cases that may result in complete loss of body and scalp hair. Objectives: The present study aimed to compare the effectiveness of topical calcipotriol, intralesional autologous platelet-rich plasma (PRP) injection, and a combination of topical calcipotriol with intralesional autologous PRP injection in patients with AA. Methods: In this randomized clinical trial, 78 patients with AA were divided into three groups. The first group received topical calcipotriol 0.005% twice daily for three months with follow-up. The second group underwent intralesional PRP injection for six consecutive sessions at two-week intervals. The third group received both treatments. Results: A substantial reduction in the average Severity of Alopecia Tool (SALT) score was observed in all three groups (P-value = 0.001) following treatment. The absolute reductions were 3.73 points in the calcipotriol group, 6.87 points in the PRP group, and 18.98 points in the combination group. The reduction was significant (P-value = 0.001), most pronounced in the combination group, followed by the PRP group, and then the calcipotriol group. A notable decline in dermoscopic results was observed post-treatment across all three groups. Conclusions: This study concluded that topical calcipotriol, intralesional autologous PRP injection, and their combination were significantly effective in reducing SALT scores in patients with AA. This reduction was most evident in the combination group, followed by the PRP group, and then the calcipotriol group.
Abstract licence: CC BY-NC 4.0
Cai L, Zhang F, Zhang G, et al.
2026
Karat TP, Bains A, Bhardwaj A, et al.
2025
- Alopecia Areata
- Calcitriol
- Triamcinolone Acetonide
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
The precise mechanism of calcipotriol in remitting psoriasis is not well-underst…
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
6%
Metabolism
Elimination
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medicines. Always consult a healthcare professional.
Showing 17 of 17 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
PMID:10678179 PMID:15728261 PMID:16913708 PMID:28698609 PMID:37478846
Enters the nucleus upon vitamin D3 binding where it forms heterodimers with the retinoid X receptor/RXR .
PMID:28698609
The VDR-RXR heterodimers bind to specific response elements on DNA and activate the transcription of vitamin D3-responsive target genes .
PMID:28698609
Plays a central role in calcium homeostasis (By similarity). Also functions as a receptor for the secondary bile acid lithocholic acid (LCA) and its metabolites PMID:12016314 PMID:32354638
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC D05AX52
ATC D05AX02
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)
Calcipotriol
Additional database identifiers
Drugs Product Database (DPD)
894
ChemSpider
4450880
BindingDB
50369964
PDB
MC9
Guide to Pharmacology
2778
ZINC
ZINC000003921872
HUGO Gene Nomenclature Committee (HGNC)
HGNC:12679
GenAtlas
VDR
GeneCards
VDR
GenBank Gene Database
J03258
GenBank Protein Database
340203
Guide to Pharmacology
605
UniProt Accession
VDR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:7218
GenAtlas
MPO
GeneCards
MPO
GenBank Gene Database
J02694
GenBank Protein Database
189040
Guide to Pharmacology
2789
UniProt Accession
PERM_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2602
GenAtlas
CYP24A1
GeneCards
CYP24A1
GenBank Gene Database
L13286
GenBank Protein Database
306704
Guide to Pharmacology
1365
UniProt Accession
CP24A_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72