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Improvements in Plaque Psoriasis Associated with Calcipotriol/Betamethasone Aerosol Foam Treatment: A Post Hoc Analysis of Non-interventional Studies and Clinical Experience.
Gerdes, Sascha; Campanati, Anna; Ratzinger, Gudrun; Halioua, Bruno; Krogager Eeg, Martin; Pesiridis, Georgios; Jablonski Bernasconi, Marie Y; Lazaridou, Elizabeth.
Afiliação
  • Gerdes S; Center for Inflammatory Skin Diseases, Department of Dermatology, University Medical Center Schleswig-Holstein Campus Kiel, Kiel, Germany.
  • Campanati A; Dermatology Unit, Department of Clinical and Molecular Sciences, Polytechnic Marche University, Via Conca 70, 60020, Ancona, Italy. anna.campanati@gmail.com.
  • Ratzinger G; Department of Dermatology, Venereology and Allergology, Medical University Innsbruck, Innsbruck, Austria.
  • Halioua B; Maison de la Dermatologie, Société Française des Sciences Humaines de la Peau, Paris, France.
  • Krogager Eeg M; LEO Pharma A/S, Ballerup, Denmark.
  • Pesiridis G; LEO Pharma A/S, Ballerup, Denmark.
  • Jablonski Bernasconi MY; LEO Pharma A/S, Ballerup, Denmark.
  • Lazaridou E; 2nd Department of Dermatology-Venereology, Aristotle University School of Medicine, Thessaloniki, Greece.
Dermatol Ther (Heidelb) ; 14(3): 793-804, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38361013
ABSTRACT

INTRODUCTION:

Plaque psoriasis is a chronic relapsing inflammatory skin disease that is associated with extensive disease burden that often requires long-term therapy. Treatment of psoriasis with 4 weeks of the aerosol foam formulation of calcipotriol/betamethasone dipropionate (Cal/BD; Enstilar®, LEO Pharma) has been demonstrated to be effective, well tolerated, and associated with high patient satisfaction. Cal/BD foam is approved as a first-line treatment in multiple countries, where several non-interventional studies (NIS) have corroborated the beneficial efficacy and safety profiles determined in the randomized clinical trials. Heterogenicity in these NIS, however, prevents the use of a data pooling strategy for comparisons of effectiveness outcomes across different patient populations.

METHODS:

Therefore, here, we report on a post hoc analysis of effectiveness data consolidated from six prospective NIS to discern any differences in improvement in signs and symptoms of psoriasis attributable to Cal/BD foam treatment across the countries. In addition, we provide real-world experience of clinicians with Cal/BD foam treatment, factoring in changes in usage since these NIS were performed in their local markets.

RESULTS:

This post hoc analysis of Cal/BD foam NIS brings together data outside of randomized clinical trials from six countries to provide real-world evidence in 1388 patients showing that 4 weeks of Cal/BD foam is an effective and safe treatment option with quick onset of action for patients with psoriasis.

CONCLUSION:

These results show that regardless of NIS location, Cal/BD foam remains a well-tolerated, efficacious option for patient care that could be used as a first-line topical therapy for mild-to-severe psoriasis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: Dermatol Ther (Heidelb) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Risk_factors_studies Idioma: En Revista: Dermatol Ther (Heidelb) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha
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