Superiority of ivermectin 1% cream over metronidazole 0·75% cream in treating inflammatory lesions of rosacea: a randomized, investigator-blinded trial

Summary Background Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). Objectives To demonstrate superiority of once‐daily ivermectin 1% cream (IVM 1%) once daily vs. twice‐daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammator...

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Published inBritish journal of dermatology (1951) Vol. 172; no. 4; pp. 1103 - 1110
Main Authors Taieb, A., Ortonne, J.P., Ruzicka, T., Roszkiewicz, J., Berth-Jones, J., Peirone, M.H., Jacovella, J.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.04.2015
Subjects
Online AccessGet full text
ISSN0007-0963
1365-2133
1365-2133
DOI10.1111/bjd.13408

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Abstract Summary Background Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). Objectives To demonstrate superiority of once‐daily ivermectin 1% cream (IVM 1%) once daily vs. twice‐daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammatory lesions in subjects with moderate to severe PPR. Methods In this Phase 3, investigator‐blinded, randomized, parallel‐group study, subjects received IVM 1% once daily, or MTZ 0·75% twice daily over 16 weeks. Efficacy assessments were inflammatory lesion counts and Investigator's Global Assessment (IGA). Safety assessments included incidence of adverse events (AEs) and local tolerance parameters. Subjects evaluated their disease following a 5‐grade scale and completed questionnaires. Results A total of 962 subjects were randomized to receive IVM 1% (n = 478) or MTZ 0·75% (n = 484). At week 16, IVM 1% was significantly superior to MTZ 0·75% in terms of reduction from baseline in inflammatory lesions (83·0% vs. 73·7%; P < 0.001), observed as early as week 3 (Last Observation Carried Forward, LOCF). IGA results (subjects ‘clear’ or ‘almost clear’) also favoured IVM 1%: 84·9% vs. 75·4%, respectively (P < 0.001). Incidence of AEs was comparable between groups and local tolerability was better for IVM 1%. More subjects receiving IVM rated their global improvement as ‘excellent’ or ‘good.’ Conclusions Ivermectin 1% cream was significantly superior to MTZ 0·75% cream and achieved high patient satisfaction. What's already known about this topic? Few therapeutic alternatives currently exist in treating papulopustular rosacea (PPR). What does this study add? Ivermectin 1% cream (IVM 1%) once daily was significantly superior to metronidazole 0·75% cream (MTZ 0.75%) twice‐daily, in reducing inflammatory lesion counts, as early as week 3 and through 4 months of treatment. IVM 1% cream can be considered an effective anti‐inflammatory treatment for PPR.
AbstractList Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR).BACKGROUNDFew therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR).To demonstrate superiority of once-daily ivermectin 1% cream (IVM 1%) once daily vs. twice-daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammatory lesions in subjects with moderate to severe PPR.OBJECTIVESTo demonstrate superiority of once-daily ivermectin 1% cream (IVM 1%) once daily vs. twice-daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammatory lesions in subjects with moderate to severe PPR.In this Phase 3, investigator-blinded, randomized, parallel-group study, subjects received IVM 1% once daily, or MTZ 0·75% twice daily over 16 weeks. Efficacy assessments were inflammatory lesion counts and Investigator's Global Assessment (IGA). Safety assessments included incidence of adverse events (AEs) and local tolerance parameters. Subjects evaluated their disease following a 5-grade scale and completed questionnaires.METHODSIn this Phase 3, investigator-blinded, randomized, parallel-group study, subjects received IVM 1% once daily, or MTZ 0·75% twice daily over 16 weeks. Efficacy assessments were inflammatory lesion counts and Investigator's Global Assessment (IGA). Safety assessments included incidence of adverse events (AEs) and local tolerance parameters. Subjects evaluated their disease following a 5-grade scale and completed questionnaires.A total of 962 subjects were randomized to receive IVM 1% (n = 478) or MTZ 0·75% (n = 484). At week 16, IVM 1% was significantly superior to MTZ 0·75% in terms of reduction from baseline in inflammatory lesions (83·0% vs. 73·7%; P < 0.001), observed as early as week 3 (Last Observation Carried Forward, LOCF). IGA results (subjects 'clear' or 'almost clear') also favoured IVM 1%: 84·9% vs. 75·4%, respectively (P < 0.001). Incidence of AEs was comparable between groups and local tolerability was better for IVM 1%. More subjects receiving IVM rated their global improvement as 'excellent' or 'good.'RESULTSA total of 962 subjects were randomized to receive IVM 1% (n = 478) or MTZ 0·75% (n = 484). At week 16, IVM 1% was significantly superior to MTZ 0·75% in terms of reduction from baseline in inflammatory lesions (83·0% vs. 73·7%; P < 0.001), observed as early as week 3 (Last Observation Carried Forward, LOCF). IGA results (subjects 'clear' or 'almost clear') also favoured IVM 1%: 84·9% vs. 75·4%, respectively (P < 0.001). Incidence of AEs was comparable between groups and local tolerability was better for IVM 1%. More subjects receiving IVM rated their global improvement as 'excellent' or 'good.'Ivermectin 1% cream was significantly superior to MTZ 0·75% cream and achieved high patient satisfaction.CONCLUSIONSIvermectin 1% cream was significantly superior to MTZ 0·75% cream and achieved high patient satisfaction.
Summary Background Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). Objectives To demonstrate superiority of once‐daily ivermectin 1% cream (IVM 1%) once daily vs. twice‐daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammatory lesions in subjects with moderate to severe PPR. Methods In this Phase 3, investigator‐blinded, randomized, parallel‐group study, subjects received IVM 1% once daily, or MTZ 0·75% twice daily over 16 weeks. Efficacy assessments were inflammatory lesion counts and Investigator's Global Assessment (IGA). Safety assessments included incidence of adverse events (AEs) and local tolerance parameters. Subjects evaluated their disease following a 5‐grade scale and completed questionnaires. Results A total of 962 subjects were randomized to receive IVM 1% (n = 478) or MTZ 0·75% (n = 484). At week 16, IVM 1% was significantly superior to MTZ 0·75% in terms of reduction from baseline in inflammatory lesions (83·0% vs. 73·7%; P < 0.001), observed as early as week 3 (Last Observation Carried Forward, LOCF). IGA results (subjects ‘clear’ or ‘almost clear’) also favoured IVM 1%: 84·9% vs. 75·4%, respectively (P < 0.001). Incidence of AEs was comparable between groups and local tolerability was better for IVM 1%. More subjects receiving IVM rated their global improvement as ‘excellent’ or ‘good.’ Conclusions Ivermectin 1% cream was significantly superior to MTZ 0·75% cream and achieved high patient satisfaction. What's already known about this topic? Few therapeutic alternatives currently exist in treating papulopustular rosacea (PPR). What does this study add? Ivermectin 1% cream (IVM 1%) once daily was significantly superior to metronidazole 0·75% cream (MTZ 0.75%) twice‐daily, in reducing inflammatory lesion counts, as early as week 3 and through 4 months of treatment. IVM 1% cream can be considered an effective anti‐inflammatory treatment for PPR.
Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). To demonstrate superiority of once-daily ivermectin 1% cream (IVM 1%) once daily vs. twice-daily metronidazole (MTZ 0·75%) cream, regarding percentage reduction of inflammatory lesions in subjects with moderate to severe PPR. In this Phase 3, investigator-blinded, randomized, parallel-group study, subjects received IVM 1% once daily, or MTZ 0·75% twice daily over 16 weeks. Efficacy assessments were inflammatory lesion counts and Investigator's Global Assessment (IGA). Safety assessments included incidence of adverse events (AEs) and local tolerance parameters. Subjects evaluated their disease following a 5-grade scale and completed questionnaires. A total of 962 subjects were randomized to receive IVM 1% (n = 478) or MTZ 0·75% (n = 484). At week 16, IVM 1% was significantly superior to MTZ 0·75% in terms of reduction from baseline in inflammatory lesions (83·0% vs. 73·7%; P < 0.001), observed as early as week 3 (Last Observation Carried Forward, LOCF). IGA results (subjects 'clear' or 'almost clear') also favoured IVM 1%: 84·9% vs. 75·4%, respectively (P < 0.001). Incidence of AEs was comparable between groups and local tolerability was better for IVM 1%. More subjects receiving IVM rated their global improvement as 'excellent' or 'good.' Ivermectin 1% cream was significantly superior to MTZ 0·75% cream and achieved high patient satisfaction.
Author Ruzicka, T.
Berth-Jones, J.
Ortonne, J.P.
Jacovella, J.
Roszkiewicz, J.
Peirone, M.H.
Taieb, A.
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  fullname: Roszkiewicz, J.
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  surname: Jacovella
  fullname: Jacovella, J.
  organization: Galderma R&D, Sophia Antipolis, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25228137$$D View this record in MEDLINE/PubMed
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PublicationCentury 2000
PublicationDate 2015-04
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  year: 2015
  text: 2015-04
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PublicationPlace England
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PublicationTitle British journal of dermatology (1951)
PublicationTitleAlternate Br J Dermatol
PublicationYear 2015
Publisher Blackwell Publishing Ltd
Publisher_xml – name: Blackwell Publishing Ltd
References Zhang X, Song Y, Ci X et al. Ivermectin inhibits LPS-induced production of inflammatory cytokines and improves LPS-induced survival in mice. Inflamm Res 2008; 57:524-9.
van Zuuren EJ, Kramer SF, Carter BR et al. Effective and evidence-based management strategies for rosacea: summary of a Cochrane systematic review. Br J Dermatol 2011; 165:760-81.
Augustin M, Herberger K, Hintzen S et al. Prevalence of skin lesions and need for treatment in a cohort of 90880 workers. Br J Dermatol 2011; 165:865-73.
McAleer MA, Fitzpatrick P, Powell FC. Papulopustular rosacea: prevalence and relationship to photodamage. J Am Acad Dermatol 2010; 63:33-9.
Yanagihara K, Kadoto J, Kohno S. Diffuse panbronchiolitis- pathophysiology and treatment mechanisms. Int J Antimicrob Agents 2001; 18 (Suppl. 1):S83-7.
Filho PA, Hazarbassanov RM, Grisolia AB et al. The efficacy of oral ivermectin for the treatment of chronic blepharitis in patients tested positive for Demodex spp. Br J Ophthalmol 2011; 95:893-5.
Wolstenholme AJ, Rogers AT. Glutamate-gated chloride channels and the mode of action of the avermectin/milbemycin anthelmintics. Parasitology 2005; 131 (Suppl):S85-95.
Damian D. Demodex infestation in a child with leukemia: treatment with ivermectin and permethrin. Int J Dermatol 2003; 42:724-6.
Holmes AD. Potential role of microorganisms in the pathogenesis of rosacea. J Am Acad Dermatol 2013; 69:1025-32.
Del Rosso JQ, Gallo RL, Tanghetti E et al. An evaluation of potential correlations between pathophysiologic mechanisms, clinical manifestations, and management of rosacea. Cutis 2013; 91 (Suppl 3):1-8.
Shimose L, Munoz-Price LS. Diagnosis, prevention, and treatment of scabies. Curr Infect Dis Rep 2013; 15:426-31.
Balkrishnan R, McMichael AJ, Hu JY et al. Correlates of health-related quality of life in women with severe facial blemishes. Int J Dermatol 2006; 45:111-15.
Elewski BE, Draelos Z, Dréno B et al. Rosacea - global diversity and optimized outcome: proposed international consensus from the Rosacea International Expert Group. J Eur Acad Dermatol Venereol 2011; 25:188-200.
Ianaro A, Ialenti A, Maffia P et al. Anti-inflammatory activity of macrolide antibiotics. J Pharmacol Exp Ther 2000; 292:156-63.
Stein L, Kircik L, Fowler J et al. Efficacy and safety of ivermectin 1% cream in treatment of papulopustular rosacea: results of two randomized, double-blind, vehicle-controlled pivotal studies. J Drugs Dermatol 2014; 13:316-23.
Jain A, Sangal L, Basal E et al. Anti-inflammatory effects of erythromycin and tetracycline on Propionibacterium acnes induced production of chemotactic factors and reactive oxygen species by human neutrophils. Dermatol Online J 2002; 8:2.
Finlay AY, Khan GK. Dermatology Life Quality Index (DLQI) - a simple practical measure for routine clinical use. Clin Exp Dermatol 1994; 19:210-16.
Chosidow O, Cribier B. Epidemiology of rosacea: updated data. Ann Dermatol Venereol 2011; 138 (Suppl. 3):S179-83.
Berg M, Lidén S. An epidemiological study of rosacea. Acta Derm Venereol 1989; 69:419-23.
Pariser DM, Meinking TL, Bell M, Ryan WG. Topical 0.5% ivermectin lotion for treatment of head lice. N Engl J Med 2012; 367:1687-93.
Ci X, Li H, Yu Q et al. Avermectin exerts anti-inflammatory effect by downregulating the nuclear transcription factor kappa-B and mitogen-activated protein kinase activation pathway. Fundam Clin Pharmacol 2009; 23:449-55.
Pelle MT, Crawford GH, James WD. Rosacea: II. Therapy. J Am Acad Dermatol 2004; 51:499-514.
Wilkin J, Dahl M, Detmar M et al. Standard classification of rosacea: report of the National Rosacea Society Expert Committee on the classification and staging of rosacea. J Am Acad Dermatol 2002; 46:584-7.
Forton FMN. Papulopustular rosacea, skin immunity and Demodex: pityriasis folliculorum as a missing link. J Eur Acad Dermatol Venereol 2012; 26:19-28.
2011; 138
2009; 23
2013; 15
2013; 69
2004; 51
2005; 131
2006; 45
1994; 19
2002; 46
2011; 95
2002; 8
2013; 91
2000; 292
2014; 13
2008; 57
2001; 18
2011; 25
2012; 26
2012; 367
1989; 69
2010; 63
2003; 42
2011; 165
Stein (10.1111/bjd.13408-BIB0018|bjd13408-cit-0018) 2014; 13
Forton (10.1111/bjd.13408-BIB0024|bjd13408-cit-0024) 2012; 26
Berg (10.1111/bjd.13408-BIB0002|bjd13408-cit-0002) 1989; 69
Jain (10.1111/bjd.13408-BIB0022|bjd13408-cit-0022) 2002; 8
Yanagihara (10.1111/bjd.13408-BIB0016|bjd13408-cit-0016) 2001; 18
Holmes (10.1111/bjd.13408-BIB0008|bjd13408-cit-0008) 2013; 69
Filho (10.1111/bjd.13408-BIB0014|bjd13408-cit-0014) 2011; 95
Zhang (10.1111/bjd.13408-BIB0021|bjd13408-cit-0021) 2008; 57
McAleer (10.1111/bjd.13408-BIB0003|bjd13408-cit-0003) 2010; 63
Wolstenholme (10.1111/bjd.13408-BIB0023|bjd13408-cit-0023) 2005; 131
Balkrishnan (10.1111/bjd.13408-BIB0006|bjd13408-cit-0006) 2006; 45
Ci (10.1111/bjd.13408-BIB0015|bjd13408-cit-0015) 2009; 23
Shimose (10.1111/bjd.13408-BIB0011|bjd13408-cit-0011) 2013; 15
Damian (10.1111/bjd.13408-BIB0013|bjd13408-cit-0013) 2003; 42
Wilkin (10.1111/bjd.13408-BIB0005|bjd13408-cit-0005) 2002; 46
Chosidow (10.1111/bjd.13408-BIB0001|bjd13408-cit-0001) 2011; 138
Pariser (10.1111/bjd.13408-BIB0012|bjd13408-cit-0012) 2012; 367
Zuuren (10.1111/bjd.13408-BIB0010|bjd13408-cit-0010) 2011; 165
Ianaro (10.1111/bjd.13408-BIB0017|bjd13408-cit-0017) 2000; 292
Finlay (10.1111/bjd.13408-BIB0019|bjd13408-cit-0019) 1994; 19
Elewski (10.1111/bjd.13408-BIB0020|bjd13408-cit-0020) 2011; 25
Augustin (10.1111/bjd.13408-BIB0004|bjd13408-cit-0004) 2011; 165
Del Rosso (10.1111/bjd.13408-BIB0007|bjd13408-cit-0007) 2013; 91
Pelle (10.1111/bjd.13408-BIB0009|bjd13408-cit-0009) 2004; 51
References_xml – reference: McAleer MA, Fitzpatrick P, Powell FC. Papulopustular rosacea: prevalence and relationship to photodamage. J Am Acad Dermatol 2010; 63:33-9.
– reference: Stein L, Kircik L, Fowler J et al. Efficacy and safety of ivermectin 1% cream in treatment of papulopustular rosacea: results of two randomized, double-blind, vehicle-controlled pivotal studies. J Drugs Dermatol 2014; 13:316-23.
– reference: Augustin M, Herberger K, Hintzen S et al. Prevalence of skin lesions and need for treatment in a cohort of 90880 workers. Br J Dermatol 2011; 165:865-73.
– reference: Filho PA, Hazarbassanov RM, Grisolia AB et al. The efficacy of oral ivermectin for the treatment of chronic blepharitis in patients tested positive for Demodex spp. Br J Ophthalmol 2011; 95:893-5.
– reference: Ianaro A, Ialenti A, Maffia P et al. Anti-inflammatory activity of macrolide antibiotics. J Pharmacol Exp Ther 2000; 292:156-63.
– reference: Berg M, Lidén S. An epidemiological study of rosacea. Acta Derm Venereol 1989; 69:419-23.
– reference: Ci X, Li H, Yu Q et al. Avermectin exerts anti-inflammatory effect by downregulating the nuclear transcription factor kappa-B and mitogen-activated protein kinase activation pathway. Fundam Clin Pharmacol 2009; 23:449-55.
– reference: Wilkin J, Dahl M, Detmar M et al. Standard classification of rosacea: report of the National Rosacea Society Expert Committee on the classification and staging of rosacea. J Am Acad Dermatol 2002; 46:584-7.
– reference: Pelle MT, Crawford GH, James WD. Rosacea: II. Therapy. J Am Acad Dermatol 2004; 51:499-514.
– reference: Zhang X, Song Y, Ci X et al. Ivermectin inhibits LPS-induced production of inflammatory cytokines and improves LPS-induced survival in mice. Inflamm Res 2008; 57:524-9.
– reference: van Zuuren EJ, Kramer SF, Carter BR et al. Effective and evidence-based management strategies for rosacea: summary of a Cochrane systematic review. Br J Dermatol 2011; 165:760-81.
– reference: Forton FMN. Papulopustular rosacea, skin immunity and Demodex: pityriasis folliculorum as a missing link. J Eur Acad Dermatol Venereol 2012; 26:19-28.
– reference: Shimose L, Munoz-Price LS. Diagnosis, prevention, and treatment of scabies. Curr Infect Dis Rep 2013; 15:426-31.
– reference: Pariser DM, Meinking TL, Bell M, Ryan WG. Topical 0.5% ivermectin lotion for treatment of head lice. N Engl J Med 2012; 367:1687-93.
– reference: Finlay AY, Khan GK. Dermatology Life Quality Index (DLQI) - a simple practical measure for routine clinical use. Clin Exp Dermatol 1994; 19:210-16.
– reference: Jain A, Sangal L, Basal E et al. Anti-inflammatory effects of erythromycin and tetracycline on Propionibacterium acnes induced production of chemotactic factors and reactive oxygen species by human neutrophils. Dermatol Online J 2002; 8:2.
– reference: Damian D. Demodex infestation in a child with leukemia: treatment with ivermectin and permethrin. Int J Dermatol 2003; 42:724-6.
– reference: Balkrishnan R, McMichael AJ, Hu JY et al. Correlates of health-related quality of life in women with severe facial blemishes. Int J Dermatol 2006; 45:111-15.
– reference: Holmes AD. Potential role of microorganisms in the pathogenesis of rosacea. J Am Acad Dermatol 2013; 69:1025-32.
– reference: Elewski BE, Draelos Z, Dréno B et al. Rosacea - global diversity and optimized outcome: proposed international consensus from the Rosacea International Expert Group. J Eur Acad Dermatol Venereol 2011; 25:188-200.
– reference: Wolstenholme AJ, Rogers AT. Glutamate-gated chloride channels and the mode of action of the avermectin/milbemycin anthelmintics. Parasitology 2005; 131 (Suppl):S85-95.
– reference: Chosidow O, Cribier B. Epidemiology of rosacea: updated data. Ann Dermatol Venereol 2011; 138 (Suppl. 3):S179-83.
– reference: Del Rosso JQ, Gallo RL, Tanghetti E et al. An evaluation of potential correlations between pathophysiologic mechanisms, clinical manifestations, and management of rosacea. Cutis 2013; 91 (Suppl 3):1-8.
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  start-page: 449
  year: 2009
  ident: 10.1111/bjd.13408-BIB0015|bjd13408-cit-0015
  article-title: Avermectin exerts anti-inflammatory effect by downregulating the nuclear transcription factor kappa-B and mitogen-activated protein kinase activation pathway
  publication-title: Fundam Clin Pharmacol
  doi: 10.1111/j.1472-8206.2009.00684.x
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Snippet Summary Background Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). Objectives To demonstrate superiority of...
Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR). To demonstrate superiority of once-daily ivermectin 1% cream...
Few therapeutic alternatives currently exist in the treatment of papulopustular rosacea (PPR).BACKGROUNDFew therapeutic alternatives currently exist in the...
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SubjectTerms Administration, Cutaneous
Adolescent
Adult
Aged
Aged, 80 and over
Dermatologic Agents - administration & dosage
Dermatologic Agents - adverse effects
Female
Humans
Ivermectin - administration & dosage
Ivermectin - adverse effects
Male
Metronidazole - administration & dosage
Metronidazole - adverse effects
Middle Aged
Ointments
Patient Satisfaction
Rosacea - drug therapy
Treatment Outcome
Young Adult
Title Superiority of ivermectin 1% cream over metronidazole 0·75% cream in treating inflammatory lesions of rosacea: a randomized, investigator-blinded trial
URI https://api.istex.fr/ark:/67375/WNG-TV201ZFR-5/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fbjd.13408
https://www.ncbi.nlm.nih.gov/pubmed/25228137
https://www.proquest.com/docview/1669451232
Volume 172
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