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
dc.contributor.author | Taieb, A | |
dc.contributor.author | Khemis, A | |
dc.contributor.author | Ruzicka, T | |
dc.contributor.author | Barańska-Rybak, W | |
dc.contributor.author | Berth-Jones, J | |
dc.contributor.author | Schauber, J | |
dc.contributor.author | Briantais, P | |
dc.contributor.author | Jacovella, J | |
dc.contributor.author | Passeron, T | |
dc.contributor.other | Ivermectin Phase III Study Group | |
dc.date.accessioned | 2024-06-10T11:06:30Z | |
dc.date.available | 2024-06-10T11:06:30Z | |
dc.date.issued | 2016-05 | |
dc.identifier.citation | Taieb 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.issn | 0926-9959 | |
dc.identifier.doi | 10.1111/jdv.13537 | |
dc.identifier.pmid | 26691278 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14200/4827 | |
dc.description.abstract | Background: 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.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Dermatology | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dc.source.journaltitle | Journal of the European Academy of Dermatology and Venereology | en_US |
rioxxterms.version | NA | en_US |
rioxxterms.type | Article | en_US |
dc.contributor.trustauthor | Berth-Jones, J. | |
dc.contributor.department | Dermatology | en_US |
dc.contributor.role | Medical and Dental | en_US |
dc.contributor.affiliation | Hôpital 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, France | en_US |
oa.grant.openaccess | na | en_US |