Ozenoxacin, a New Effective and Safe Topical Treatment for Impetigo in Children and Adolescents.


Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2020
Historique:
received: 16 07 2019
accepted: 04 11 2019
pubmed: 21 1 2020
medline: 12 9 2020
entrez: 21 1 2020
Statut: ppublish

Résumé

Ozenoxacin is a topical antibiotic approved in Europe to treat non-bullous impetigo in adults and children aged ≥6 months. This analysis evaluated the efficacy and safety of ozenoxacin in paediatric patients by age group. Pooled data for patients aged 6 months to <18 years who had participated in a phase I or in two phase III clinical trials of ozenoxacin 1% cream were analysed by age group: 0.5-<2, 2-<6, 6-<12, and 12-<18 years. The combined population comprised 529 patients with non-bullous impetigo treated with ozenoxacin (n = 239), vehicle (n = 201), or retapamulin as internal validation control (n = 89). Studies were well matched for extent and severity of impetigo and therapeutic schedule (twice daily application for 5 days). The clinical success rate after 5 days' treatment (day 6-7, end of therapy), and microbiological success rates after 3-4 days' treatment and at the end of therapy, were significantly higher with ozenoxacin than vehicle (p < 0.0001 for all comparisons). Clinical and bacterial eradication rates were higher with ozenoxacin than vehicle in each age group. No safety concerns were identified with ozenoxacin. One (0.3%) of 327 plasma samples exceeded the lower limit of quantification for ozenoxacin, but the low concentration indicated negligible systemic absorption. This combined analysis supports the efficacy and safety of ozenoxacin administered twice daily for 5 days. Ozenoxacin 1% cream is a new option to consider for treatment of non-bullous impetigo in children aged 6 months to <18 years.

Sections du résumé

BACKGROUND BACKGROUND
Ozenoxacin is a topical antibiotic approved in Europe to treat non-bullous impetigo in adults and children aged ≥6 months. This analysis evaluated the efficacy and safety of ozenoxacin in paediatric patients by age group.
METHODS METHODS
Pooled data for patients aged 6 months to <18 years who had participated in a phase I or in two phase III clinical trials of ozenoxacin 1% cream were analysed by age group: 0.5-<2, 2-<6, 6-<12, and 12-<18 years.
RESULTS RESULTS
The combined population comprised 529 patients with non-bullous impetigo treated with ozenoxacin (n = 239), vehicle (n = 201), or retapamulin as internal validation control (n = 89). Studies were well matched for extent and severity of impetigo and therapeutic schedule (twice daily application for 5 days). The clinical success rate after 5 days' treatment (day 6-7, end of therapy), and microbiological success rates after 3-4 days' treatment and at the end of therapy, were significantly higher with ozenoxacin than vehicle (p < 0.0001 for all comparisons). Clinical and bacterial eradication rates were higher with ozenoxacin than vehicle in each age group. No safety concerns were identified with ozenoxacin. One (0.3%) of 327 plasma samples exceeded the lower limit of quantification for ozenoxacin, but the low concentration indicated negligible systemic absorption.
CONCLUSION CONCLUSIONS
This combined analysis supports the efficacy and safety of ozenoxacin administered twice daily for 5 days. Ozenoxacin 1% cream is a new option to consider for treatment of non-bullous impetigo in children aged 6 months to <18 years.

Identifiants

pubmed: 31958794
pii: 000504536
doi: 10.1159/000504536
pmc: PMC7257257
doi:

Substances chimiques

Aminopyridines 0
Anti-Bacterial Agents 0
Quinolones 0
ozenoxacin V0LH498RFO

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase III Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

199-207

Informations de copyright

The Author(s). Published by S. Karger AG, Basel.

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Auteurs

Antonio Torrelo (A)

Department of Dermatology, Children's Hospital del Niño Jesús, Madrid, Spain.

Ramon Grimalt (R)

Universitat Internacional de Catalunya, Barcelona, Spain.

Xavier Masramon (X)

SAIL (Servicio de Asesoría a la Investigación y Logística) SL, Barcelona, Spain.

Núria Albareda López (N)

Clinical Research Department, Ferrer Internacional SA, Barcelona, Spain.

Ilonka Zsolt (I)

Medical Department, Ferrer Internacional SA, Barcelona, Spain, izsolt@ferrer.com.

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Classifications MeSH