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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorZalacain Vicuña, Antonio Jesús
dc.contributor.authorNieto, Carlos
dc.contributor.authorPicas, Jordi
dc.contributor.authorMartínez-Serrano, Helena
dc.contributor.authorBermejo, Rafael
dc.contributor.authorCorrales, Adrián
dc.contributor.authorGarcia-Patos Briones, Vicente
dc.date.accessioned2025-01-31T12:19:56Z
dc.date.available2025-01-31T12:19:56Z
dc.date.copyright2022
dc.date.issued2023-07
dc.identifier.citationZalacain-Vicuña AJ, Nieto C, Picas J, Martínez H, Bermejo R, Corrales A, et al. Efficacy and safety of a new medicated nail hydrolacquer in the treatment of adults with toenail onychomycosis: A randomised clinical trial. Mycoses. 2023 Jul;66(7):566–75.
dc.identifier.issn1439-0507
dc.identifier.urihttps://hdl.handle.net/11351/12512
dc.descriptionMycological cure; Onychomycosis; Water-soluble nail lacquer
dc.description.abstractBackground A new water-soluble formulation with ciclopirox has shown a higher penetration than other ciclopirox nail lacquers currently marketed, thus providing a higher concentration of ciclopirox into the nail. Objective To evaluate the efficacy and safety of a new ciclopirox nail hydrolacquer compared with its vehicle and an active comparator (hydroxypropyl chitosan-based 80 mg/g ciclopirox nail lacquer) for the treatment of toenail fungal infection. Methods Phase III, multicenter, randomised, double-blind, clinical trial in patients with distal mild to moderate toenail onychomycosis due to dermatophyte fungi. Patients were randomised to apply topically a ciclopirox nail hydrolacquer, its vehicle or a reference product once daily for 48 weeks with a follow-up period of 4 weeks up to week 52. Results A total of 381 patients were included. No statistically significant differences were observed between patient groups in the proportion of subjects achieving a complete cure. At week 52, a higher percentage of patients in the ciclopirox nail hydrolacquer group achieved a mycological cure (negative for culture and DTS/KOH test, with results: 32.0% ciclopirox nail hydrolacquer, 23.2% vehicle and 27% reference product, respectively), and similar results were found for improvement (mycological cure and reduction of diseased nail ≥20%, with results: 27.2% ciclopirox nail hydrolacquer, 21.6% vehicle and 20.6% reference product, respectively). Regarding mycological results, only ciclopirox nail hydrolacquer demonstrated significant statistical superiority versus vehicle negativizing dermatophyte culture (p = .039) with no recurrences, relapses or re-infections in a four-week follow-up patients with complete cure. The safety profile was comparable to the vehicle and reference product and consistent with the previously reported. Conclusions A new water-soluble formulation for a ciclopirox nail lacquer showed similar efficacy to the reference product to eradicate toenail onychomycosis and superiority in the mycological cure defined by negative culture, thus preventing reinfections and recurrences. Efficacy and safety data demonstrate the positive benefit–risk profile of this new topical antifungal preparation. [Correction added on 13 April 2023, after first online publication: The results and conclusions in the Abstract contained incorrect information and were revised in this version.]
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesMycoses;66(7)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectMedicaments antifúngics - Ús terapèutic
dc.subjectOnicomicosi - Tractament
dc.subjectUngles
dc.subject.meshTreatment Outcome
dc.subject.meshOnychomycosis
dc.subject.mesh/drug therapy
dc.subject.meshAntifungal Agents
dc.subject.mesh/therapeutic use
dc.subject.meshNails
dc.titleEfficacy and safety of a new medicated nail hydrolacquer in the treatment of adults with toenail onychomycosis: A randomised clinical trial
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1111/myc.13543
dc.subject.decsresultado del tratamiento
dc.subject.decsonicomicosis
dc.subject.decs/farmacoterapia
dc.subject.decsantifúngicos
dc.subject.decs/uso terapéutico
dc.subject.decsuñas
dc.relation.publishversionhttps://doi.org/10.1111/myc.13543
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Zalacain-Vicuña AJ] Podiatry School. Faculty of Medicine and Health Sciences, University of Barcelona, L'Hospitalet de Llobregat, Spain. [Nieto C, Picas J, Martínez H, Bermejo R, Corrales A] Laboratorio Reig Jofre, Barcelona, Spain. [García-Patos Briones V] Servei de Dermatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma of Barcelona, Bellaterra, Spain
dc.identifier.pmid36336989
dc.identifier.wos000888910300001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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