Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies

Yan Li,1 Maria Palmisano,1 Duxin Sun,2 Simon Zhou1 1Translational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ 07920, USA; 2Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USACorrespondence: Simon ZhouTranslational De...

Full description

Bibliographic Details
Main Authors: Li Y, Palmisano M, Sun D, Zhou S
Format: Article
Language:English
Published: Dove Medical Press 2020-07-01
Series:Clinical Pharmacology: Advances and Applications
Subjects:
Online Access:https://www.dovepress.com/pharmacokinetic-disposition-difference-between-cyclosporine-and-voclos-peer-reviewed-article-CPAA
_version_ 1818842460524118016
author Li Y
Palmisano M
Sun D
Zhou S
author_facet Li Y
Palmisano M
Sun D
Zhou S
author_sort Li Y
collection DOAJ
description Yan Li,1 Maria Palmisano,1 Duxin Sun,2 Simon Zhou1 1Translational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ 07920, USA; 2Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USACorrespondence: Simon ZhouTranslational Development and Clinical Pharmacology, Celgene Corporation, 556 Morris Avenue, Summit, NJ 07920, USATel +1 908-673-9284Fax +1 908-673-2842Email szhou@celgene.comBackground: Voclosporin, a more potent derivative of cyclosporine, has been studied extensively in patients with immunologic disorders such as psoriasis, organ transplantation, uvetitis and lupus nephritis. Although better tolerated and safer than cyclosporine, voclosporin is inferior to cyclosporine in treating psoriasis, non-inferior to tacrolimus in organ transplantation and efficacious in treating lupus nephritis.Methods: The pharmacokinetic dispositions of voclosporin and cyclosporine in central and peripheral compartments were analyzed and correlated with their distinct clinical efficacy and safety profiles.Results: Both drugs demonstrated non-linear pharmacokinetics with increasing doses, more prominently at lower doses of voclosporin than at 10-fold higher doses of cyclosporine. Repeated lower dosing of voclosporin produced preferential calcineurin inhibition in and near blood circulation, leading to relatively lower cardiovascular and renal adverse effects but inferior efficacy for psoriasis compared to cyclosporine. With 10-fold higher plasma levels and deeper tissue penetration, cyclosporine has more prevalent renal and cardiac toxicities but superior efficacy to treat psoriasis.Conclusion: Although the two drugs are similar in structure and mechanism of action, the high potency and low dose compounded by the non-linear disposition of voclosporin resulted in more systemic versus local calcineurin inhibition than with cyclosporine. The dispositional difference between voclosporin and cyclosporine accounted for the puzzling efficacy and safety observations in different patients and was the basis for their optimal and differential use in treating diverse immunologic disorders.Keywords: pharmacokinetic, disposition, cyclosporine and voclosporin
first_indexed 2024-12-19T04:42:20Z
format Article
id doaj.art-2d8644db28da449d8f59566a08ebf544
institution Directory Open Access Journal
issn 1179-1438
language English
last_indexed 2024-12-19T04:42:20Z
publishDate 2020-07-01
publisher Dove Medical Press
record_format Article
series Clinical Pharmacology: Advances and Applications
spelling doaj.art-2d8644db28da449d8f59566a08ebf5442022-12-21T20:35:35ZengDove Medical PressClinical Pharmacology: Advances and Applications1179-14382020-07-01Volume 12839654986Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical StudiesLi YPalmisano MSun DZhou SYan Li,1 Maria Palmisano,1 Duxin Sun,2 Simon Zhou1 1Translational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ 07920, USA; 2Department of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USACorrespondence: Simon ZhouTranslational Development and Clinical Pharmacology, Celgene Corporation, 556 Morris Avenue, Summit, NJ 07920, USATel +1 908-673-9284Fax +1 908-673-2842Email szhou@celgene.comBackground: Voclosporin, a more potent derivative of cyclosporine, has been studied extensively in patients with immunologic disorders such as psoriasis, organ transplantation, uvetitis and lupus nephritis. Although better tolerated and safer than cyclosporine, voclosporin is inferior to cyclosporine in treating psoriasis, non-inferior to tacrolimus in organ transplantation and efficacious in treating lupus nephritis.Methods: The pharmacokinetic dispositions of voclosporin and cyclosporine in central and peripheral compartments were analyzed and correlated with their distinct clinical efficacy and safety profiles.Results: Both drugs demonstrated non-linear pharmacokinetics with increasing doses, more prominently at lower doses of voclosporin than at 10-fold higher doses of cyclosporine. Repeated lower dosing of voclosporin produced preferential calcineurin inhibition in and near blood circulation, leading to relatively lower cardiovascular and renal adverse effects but inferior efficacy for psoriasis compared to cyclosporine. With 10-fold higher plasma levels and deeper tissue penetration, cyclosporine has more prevalent renal and cardiac toxicities but superior efficacy to treat psoriasis.Conclusion: Although the two drugs are similar in structure and mechanism of action, the high potency and low dose compounded by the non-linear disposition of voclosporin resulted in more systemic versus local calcineurin inhibition than with cyclosporine. The dispositional difference between voclosporin and cyclosporine accounted for the puzzling efficacy and safety observations in different patients and was the basis for their optimal and differential use in treating diverse immunologic disorders.Keywords: pharmacokinetic, disposition, cyclosporine and voclosporinhttps://www.dovepress.com/pharmacokinetic-disposition-difference-between-cyclosporine-and-voclos-peer-reviewed-article-CPAApharmacokineticdispositioncyclosporine and voclosporin
spellingShingle Li Y
Palmisano M
Sun D
Zhou S
Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
Clinical Pharmacology: Advances and Applications
pharmacokinetic
disposition
cyclosporine and voclosporin
title Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
title_full Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
title_fullStr Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
title_full_unstemmed Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
title_short Pharmacokinetic Disposition Difference Between Cyclosporine and Voclosporin Drives Their Distinct Efficacy and Safety Profiles in Clinical Studies
title_sort pharmacokinetic disposition difference between cyclosporine and voclosporin drives their distinct efficacy and safety profiles in clinical studies
topic pharmacokinetic
disposition
cyclosporine and voclosporin
url https://www.dovepress.com/pharmacokinetic-disposition-difference-between-cyclosporine-and-voclos-peer-reviewed-article-CPAA
work_keys_str_mv AT liy pharmacokineticdispositiondifferencebetweencyclosporineandvoclosporindrivestheirdistinctefficacyandsafetyprofilesinclinicalstudies
AT palmisanom pharmacokineticdispositiondifferencebetweencyclosporineandvoclosporindrivestheirdistinctefficacyandsafetyprofilesinclinicalstudies
AT sund pharmacokineticdispositiondifferencebetweencyclosporineandvoclosporindrivestheirdistinctefficacyandsafetyprofilesinclinicalstudies
AT zhous pharmacokineticdispositiondifferencebetweencyclosporineandvoclosporindrivestheirdistinctefficacyandsafetyprofilesinclinicalstudies