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dc.contributor.authorTaieb, A
dc.contributor.authorKhemis, A
dc.contributor.authorRuzicka, T
dc.contributor.authorBarańska-Rybak, W
dc.contributor.authorBerth-Jones, J
dc.contributor.authorSchauber, J
dc.contributor.authorBriantais, P
dc.contributor.authorJacovella, J
dc.contributor.authorPasseron, T
dc.contributor.otherIvermectin Phase III Study Group
dc.date.accessioned2024-06-10T11:06:30Z
dc.date.available2024-06-10T11:06:30Z
dc.date.issued2016-05
dc.identifier.citationTaieb A, Khemis A, Ruzicka T, Barańska-Rybak W, Berth-Jones J, Schauber J, Briantais P, Jacovella J, Passeron T; Ivermectin Phase III Study Group. Maintenance of remission following successful treatment of papulopustular rosacea with ivermectin 1% cream vs. metronidazole 0.75% cream: 36-week extension of the ATTRACT randomized study. J Eur Acad Dermatol Venereol. 2016 May;30(5):829-36. doi: 10.1111/jdv.13537. Epub 2015 Dec 21.en_US
dc.identifier.issn0926-9959
dc.identifier.doi10.1111/jdv.13537
dc.identifier.pmid26691278
dc.identifier.urihttp://hdl.handle.net/20.500.14200/4827
dc.description.abstractBackground: There are a limited number of approved treatments for papulopustular rosacea (PPR) and remission is difficult to maintain after successful treatment. Objectives: To investigate remission over a 36-week extension period in patients with moderate to severe PPR successfully treated with 16 weeks' treatment with ivermectin 1% cream once daily (QD) or metronidazole 0.75% cream twice daily (BID) in a randomized, parallel-group Phase III study. Methods: Treatment was discontinued in patients initially successfully treated [Investigator's Global Assessment (IGA) score of 0 or 1] with ivermectin 1% cream QD (n = 399) or metronidazole 0.75% cream BID (n = 365; Part A) and patients were followed every 4 weeks for up to 36 weeks (Part B). Treatment with the same study treatment as used in Part A was only re-initiated if patients relapsed (IGA ≥ 2). Efficacy assessments were: time to first relapse; relapse rate; and number of days free of treatment. Safety assessments included incidence of adverse events and local cutaneous signs and symptoms. Results: The median time to first relapse was significantly longer (115 days vs. 85 days) and relapse rates at the end of the study period significantly lower (62.7% vs. 68.4%) for patients initially successfully treated with ivermectin 1% compared with metronidazole 0.75%; Kaplan-Meier plot demonstrated a statistically significant difference between the two arms (P = 0.0365). The median number of days free of treatment was higher for ivermectin compared with metronidazole (196 days vs. 169.5 days; P = 0.026). The percentage of patients who experienced a related adverse event was equally low in both groups. Conclusion: The results of this relapse study showed that an initial successful treatment with ivermectin 1% cream QD significantly extended remission of rosacea compared with initial treatment with metronidazole 0.75% cream BID following treatment cessation.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectDermatologyen_US
dc.titleMaintenance of remission following successful treatment of papulopustular rosacea with ivermectin 1% cream vs. metronidazole 0.75% cream : 36-week extension of the ATTRACT randomized studyen_US
dc.typeArticleen_US
dc.source.journaltitleJournal of the European Academy of Dermatology and Venereologyen_US
rioxxterms.versionNAen_US
rioxxterms.typeArticleen_US
dc.contributor.trustauthorBerth-Jones, J.
dc.contributor.departmentDermatologyen_US
dc.contributor.roleMedical and Dentalen_US
dc.contributor.affiliationHôpital Saint-André, Bordeaux Cedex, France; Centre Hospitalier Universitaire de Nice, France; Ludwig Maximilian University, Munich, Germany; Medical University of Gdansk, Poland; George Eliot Hospital, Nuneaton; Galderma R&D, Sophia Antipolis, Franceen_US
oa.grant.openaccessnaen_US


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