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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.
Taieb, A; Khemis, A; Ruzicka, T; Baranska-Rybak, W; Berth-Jones, J; Schauber, J; Briantais, P; Jacovella, J; Passeron, T.
Affiliation
  • Taieb A; Service de Dermatologie et Dermatologie Pédiatrique, Hôpital Saint-André, Bordeaux Cedex, France.
  • Khemis A; Dermatology Department, Centre Hospitalier Universitaire de Nice, Nice, France.
  • Ruzicka T; Department of Dermatology and Allergy, Ludwig Maximilian University, Munich, Germany.
  • Baranska-Rybak W; Department of Dermatology, Venereology and Allergology, Medical University of Gdansk Poland, Gdansk, Poland.
  • Berth-Jones J; Dermatology Clinical Research Unit, Department of Dermatology, George Eliot Hospital, Nuneaton, UK.
  • Schauber J; Department of Dermatology and Allergy, Ludwig Maximilian University, Munich, Germany.
  • Briantais P; Galderma R&D, Sophia Antipolis, France.
  • Jacovella J; Galderma R&D, Sophia Antipolis, France.
  • Passeron T; Dermatology Department, Centre Hospitalier Universitaire de Nice, Nice, France.
J Eur Acad Dermatol Venereol ; 30(5): 829-36, 2016 May.
Article in En | MEDLINE | ID: mdl-26691278
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Ivermectin / Remission Induction / Rosacea / Metronidazole Type of study: Clinical_trials Limits: Humans Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2016 Type: Article Affiliation country: France

Full text: 1 Database: MEDLINE Main subject: Ivermectin / Remission Induction / Rosacea / Metronidazole Type of study: Clinical_trials Limits: Humans Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2016 Type: Article Affiliation country: France