Voclosporin 7.9mg capsules
Requires a prescription from a doctor or prescriber
Lupus nephritis (LN) is a type of glomerulonephritis occurring in patients with systemic lupus erythematosus (SLE).
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Lupkynis 7.9mg capsules
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(2)
Voclosporin with mycophenolate mofetil for treating lupus nephritis (TA882)
Obinutuzumab with mycophenolate mofetil for treating lupus nephritis (TA1131)
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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Codes for healthcare professionals and prescribing systems
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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. 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: 6 · 2011–2026
Showing the 50 most relevant studies, sorted by most relevant.
Brad H. Rovin, Y K Onno Teng, Ellen M. Ginzler, et al.
The Lancet, 2021
- Creatinine
- Glomerular Filtration Rate
- Glucocorticoids
Patrick Ashinze, Nelson Mafua, Suvam Banerjee, et al.
Medicine, 2025
- Immunosuppressive Agents
- Lupus Erythematosus, Systemic
- Lupus Nephritis
Fei Li, Xizhe Liu, Xin-Hui Zhang, et al.
Lupus, 2025
- Lupus Nephritis
- Cyclosporine
- Immunosuppressive Agents
Basuli D, Roy S, Ray AS, et al.
2025
Abstract Background Lupus nephritis is a major cause of kidney failure worldwide, disproportionately affecting Black, Hispanic, and Asian populations. Standard regimens with mycophenolate mofetil or cyclophosphamide and glucocorticoids remain suboptimal, with many patients experiencing incomplete responses, relapses, or drug-related toxicity. Recently approved biologic and targeted therapies like belimumab, voclosporin, obinutuzumab, rituximab, have expanded treatment options, but direct comparisons of efficacy, safety, and cost are limited. Methods We conducted a systematic review of phase 2–4 randomized controlled trials enrolling adolescents or adults with biopsy-proven lupus nephritis (ISN/RPS class III–V). Eligible trials compared voclosporin, belimumab, obinutuzumab, or rituximab with placebo or standard-of-care and reported renal and/or safety outcomes with ≥ 6 months follow-up. Data were extracted on complete renal response, adverse events, infections, and mortality. Odds ratios and risk differences were calculated, and pooled estimates generated for agents with more than one trial. Cost-per-responder was estimated using U.S. drug acquisition costs. Results Six trials met inclusion criteria. Voclosporin and belimumab demonstrated consistent efficacy, with complete renal response of 30–41% at ~ 1 year, and were associated with acceptable safety. Obinutuzumab showed favorable efficacy trends in NOBILITY and REGENCY but with variable safety signals. Rituximab did not significantly improve complete renal response in the pivotal LUNAR trial. Pooled analyses indicated modest differences in safety, with belimumab having the most favorable profile. Estimated complete renal response varied widely, from ~$118,500 (rituximab) to >$214,000 (voclosporin), underscoring differences in short-term cost-efficiency. Underrepresentation of high-risk racial groups limited external validity. Conclusions Voclosporin and belimumab are supported by robust evidence and guideline endorsement. Obinutuzumab shows emerging promise but is not yet integrated in guidelines. Rituximab remains widely used off-label but lacks RCT support. This systematic review highlights efficacy, safety, and economic considerations across agents, emphasizing the need for harmonized trial design, inclusive enrollment, and cost-effectiveness analyses to ensure equitable access in LN management. Clinical trial number: not applicable
Abstract licence: CC BY
Patel JP, Hardaswani D, Chaniyara SR, et al.
2024
Lupus nephritis (LN) is a serious kidney complication associated with systemic lupus erythematosus (SLE), marked by the immune system's misdirected attack on kidney tissues, resulting in inflammation and compromised filtration. This condition has the potential to progress to end-stage renal disease in about 20% of patients within a decade of diagnosis. Lupus nephritis is more prevalent in females, highlighting the urgent need for effective treatment strategies. This systematic review consolidates findings from 16 research articles that explore various therapeutic options for LN. Key themes include the intricate pathogenesis involving immune complex deposition and the advancing treatment landscape, which encompasses both traditional immunosuppressants such as mycophenolate mofetil (MMF) and cyclophosphamide and newer biologics like belimumab and voclosporin. The review examines the efficacy and safety profiles of these treatments, underscoring the importance of personalized treatment plans based on disease severity and patient-specific factors. While newer therapies show promise for improving renal outcomes, the potential for adverse effects remains a significant concern. A thorough review was conducted to evaluate current research on lupus nephritis, focusing on treatment advancements. Two independent reviewers searched PubMed using targeted terms and MeSH categories, emphasizing studies published since 1990 identified 7898 articles from that, 16 articles met the criteria for inclusion in the study. The evaluation of bias risk was performed according to established protocols. This systematic approach provided a comprehensive analysis of recent developments in lupus nephritis therapy.
Abstract licence: CC BY
M. Lambton, E. Farrington, D. Clamp, et al.
Value in Health, 2023
N Duran, Laura Salinas-Ortega, Alberto de la Cuadra-Grande, et al.
Nephrology Dialysis Transplantation, 2025
Brad H. Rovin, Neil Solomons, William F. Pendergraft, et al.
Kidney International, 2018
- Glucocorticoids
- Immunosuppressive Agents
- Lupus Nephritis
Young Ho Lee, Gwan Gyu Song
Zeitschrift für Rheumatologie, 2021
- Lupus Nephritis
- Tacrolimus
- Network Meta-Analysis
Roberts ET, Schmajuk G, Plantinga L, et al.
2026
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
30 hours
Mechanism
Through the inhibition of calcineurin, voclosporin blocks IL-2 expression and T-…
Food interactions
2 warnings
Human targets
4 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
1.5 hours
Half-life
30 hours
[L31218]
Protein binding
97%
[L31218]
Volume of distribution
154 L
Metabolism
16.7%
Elimination
88%
[L31228]
Clearance
63.6 L/h
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Voclosporin, marketed as Lupkynis, is a calcineurin-inhibitor immunosuppressant for the treatment of LN.[L31218] This [cyclosporine] A analog was approved by the FDA on January 22, 2021 following promising results in clinical trials. Early intervention with voclosporin coupled with a kidney response is believed to prevent irreversible damage to the kidney and lead to better long-term clinical outcomes for patients with LN.[L31208] Voclosporin has demonstrated a more stable pharmacokinetic and pharmacodynamic relationship than cyclosporine, a higher potency than cyclosporine, and an improved metabolic profile when compared to older calcineurin inhibitors.[L31253]
In July 2022, the EMA's Committee for Medicinal Products for Human Use (CHMP) recommended voclosporin be granted marketing authorization for use in combination with [mycophenolate mofetil] for the treatment of adult patients with active lupus nephritis.[L43080]
[L31218]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 651 interactions
Accidental overdose with voclosporin has been reported with; symptoms of an overdose may include headache, nausea and vomiting, infections, tachycardia, urticaria, lethargy, and tremor. An increase in blood urea nitrogen, serum creatinine, and alanine aminotransferase levels is also possible. There is no known antidote to an overdose with voclosporin.
If an overdose occurs, supportive and symptomatic treatment should be initiated, in addition to discontinuation of voclosporin. Assessment of blood urea nitrogen, serum creatinine, eGFR and alanine aminotransferase levels is recommended. Prescribing information suggests contacting a poison center or medical toxicologist for the management of an overdose with voclosporin.
[L31218]
Voclospoprin is a cyclosporine A analog. It is structurally similar to cyclosporine A (CsA) with the exception of an amino acid modification in one region. This modification changes the binding of voclosporin to calcineurin. Cyclosporine inhibitors reversibly inhibit T-lymphocytes. They also inhibit lymphokine production and release. Cyclosporine A exerts its inhibitory effects on T-lymphocytes by binding to cyclophilin. A cyclophilin-cyclosporine complex is formed, leading to the inhibition of calcium- and calmodulin-dependent serine-threonine phosphatase activity of calcineurin. Along with calcineurin inhibition, the inhibition of many transcription factors necessary for the induction of various cytokine genes such as IL-2, IFN-γ, IL-4 and GM-CSF occurs. This, in turn, reduces inflammation, treating renal glomerulonephritis associated with systemic lupus erythematosus.[A227698][L31228]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L31218]
The AUC is estimated at 7693.6 ng/mL*h and the Cmax is estimated at 955.5 ng/mL.
[A227678]
[L31218]
[L31218]
[L31218]
[L31218][L31228]
[L31228]
[L31218]
Hepatic and renal impairment significantly reduce the clearance of voclosporin.
[A227708]
Proteins and enzymes this drug interacts with in the body
PMID:23041287 PMID:24392163 PMID:27226539
Together with GET1/WRB, acts as a membrane receptor for soluble GET3/TRC40, which recognizes and selectively binds the transmembrane domain of TA proteins in the cytosol .
PMID:23041287 PMID:24392163 PMID:27226539
Required for the stability of GET1 .
PMID:32187542
Stimulates calcium signaling in T cells through its involvement in elevation of intracellular calcium .
PMID:7522304
Essential for the survival of peripheral follicular B cells (By similarity)
PMID:15671020 PMID:18838687 PMID:19154138 PMID:23468591 PMID:30254215
Many of the substrates contain a PxIxIT motif and/or a LxVP motif .
PMID:17498738 PMID:17502104 PMID:22343722 PMID:23468591 PMID:27974827
In response to increased Ca(2+) levels, dephosphorylates and activates phosphatase SSH1 which results in cofilin dephosphorylation .
PMID:15671020
In response to increased Ca(2+) levels following mitochondrial depolarization, dephosphorylates DNM1L inducing DNM1L translocation to the mitochondrion .
PMID:18838687
Positively regulates the CACNA1B/CAV2.2-mediated Ca(2+) release probability at hippocampal neuronal soma and synaptic terminals (By similarity). Dephosphorylates heat shock protein HSPB1 (By similarity). Dephosphorylates and activates transcription factor NFATC1 .
PMID:19154138
In response to increased Ca(2+) levels, regulates NFAT-mediated transcription probably by dephosphorylating NFAT and promoting its nuclear translocation .
PMID:26248042
Dephosphorylates and inactivates transcription factor ELK1 .
PMID:19154138
Dephosphorylates DARPP32 .
PMID:19154138
May dephosphorylate CRTC2 at 'Ser-171' resulting in CRTC2 dissociation from 14-3-3 proteins .
PMID:30611118
Dephosphorylates transcription factor TFEB at 'Ser-211' following Coxsackievirus B3 infection, promoting nuclear translocation .
PMID:33691586
Required for postnatal development of the nephrogenic zone and superficial glomeruli in the kidneys, cell cycle homeostasis in the nephrogenic zone, and ultimately normal kidney function (By similarity).
Plays a role in intracellular AQP2 processing and localization to the apical membrane in the kidney, may thereby be required for efficient kidney filtration (By similarity). Required for secretion of salivary enzymes amylase, peroxidase, lysozyme and sialic acid via formation of secretory vesicles in the submandibular glands (By similarity). Required for calcineurin activity and homosynaptic depotentiation in the hippocampus (By similarity).
Required for normal differentiation and survival of keratinocytes and therefore required for epidermis superstructure formation (By similarity). Positively regulates osteoblastic bone formation, via promotion of osteoblast differentiation (By similarity). Positively regulates osteoclast differentiation, potentially via NFATC1 signaling (By similarity).
May play a role in skeletal muscle fiber type specification, potentially via NFATC1 signaling (By similarity). Negatively regulates MAP3K14/NIK signaling via inhibition of nuclear translocation of the transcription factors RELA and RELB (By similarity). Required for antigen-specific T-cell proliferation response (By similarity).
Dephosphorylates KLHL3, promoting the interaction between KLHL3 and WNK4 and subsequent degradation of WNK4 .
PMID:30718414
Negatively regulates SLC9A1 activity PMID:31375679
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 L04AD03
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)
Voclosporin
Additional database identifiers
ChemSpider
5293683
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1471
GenAtlas
CAMLG
GeneCards
CAMLG
GenBank Gene Database
U18242
GenBank Protein Database
619670
UniProt Accession
CAMLG_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9317
GenAtlas
PPP3R1
GeneCards
PPP3R1
GenBank Gene Database
M30773
GenBank Protein Database
180705
UniProt Accession
CANB1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9318
GenAtlas
PPP3R2
GeneCards
PPP3R2
GenBank Gene Database
AF145026
GenBank Protein Database
33150800
UniProt Accession
CANB2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9314
GeneCards
PPP3CA
GenBank Gene Database
L14778
GenBank Protein Database
306477
UniProt Accession
PP2BA_HUMAN
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: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:
- 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