Your browser doesn't support javascript.
loading
Evaluating the Efficacy, Safety, and Tolerability of the Combination of Tazarotene, Azelaic Acid, Tacrolimus, and Zinc Oxide for the Treatment of Melasma: A Pilot Study.
Kirsch, Brandon; Hoesly, Paul M; Jambusaria, Anokhi; Heckman, Michael G; Diehl, Nancy N; Sluzevich, Jason C.
Afiliação
  • Kirsch B; Drs. Kirsch (at the time of this study), Hoesly (at the time of this study), and Sluzevich are with the Department of Dermatology at the Mayo Clinic in Jacksonville, Florida.
  • Hoesly PM; Dr. Jambusaria is with the University of Texas Austin Dell Medical School in Austin, Texas.
  • Jambusaria A; Mr. Heckman and Ms. Diehl are with the Division of Biomedical Statistics and Informatics at the Mayo Clinic in Jacksonville, Florida.
  • Heckman MG; Dr. Kirsch is now in private practice with Minors Dermatology in Hollywood, Florida, and is the Medical Director and Vice President of Clinical Development at Brickell Biotech, Inc. in Boulder, Colorado.
  • Diehl NN; Dr. Hoesly is now in private practice at the Austin Regional Clinic in Austin, Texas.
  • Sluzevich JC; Drs. Kirsch (at the time of this study), Hoesly (at the time of this study), and Sluzevich are with the Department of Dermatology at the Mayo Clinic in Jacksonville, Florida.
J Clin Aesthet Dermatol ; 12(5): 40-45, 2019 May.
Article em En | MEDLINE | ID: mdl-31320976
ABSTRACT

Background:

Melasma is a common hyperpigmentation disorder of the skin. Combination therapy of topical retinoids, corticosteroids, and hydroquinone has been effective in treating melasma, but long-term use is limited by corticosteroid atrophy and exogenous ochronosis. The aim of this pilot study (NCT02730819) was to determine the efficacy, safety, and tolerability of a novel composition (2013-MCN-333) comprising tazarotene 0.075%, azelaic acid 20%, tacrolimus 0.1%, and (microfine) zinc oxide 10% for the treatment of melasma.

Methods:

Sixteen patients with moderate-to-severe melasma were treated daily with sunscreen and 2013-MCN-333 for 20 weeks. Primary outcome measure was change in Melasma Area and Severity Index (MASI) score.

Results:

Twenty-five percent of patients met the primary endpoint of a MASI score of less than eight points at Week 20. MASI score also decreased significantly from baseline (median 18.9 points) through Week 4 (median 17.3 points; p=0.006), Week 12 (median 16.0 points; p=0.001), and Week 20 (median 13.3 points; p=0.001). Treatment-related adverse events were mild, most of which decreased or resolved over the course of the study.

Limitations:

The small sample size and nonblinded nature of treatment intervention are potential limitations.

Conclusion:

Our results suggest daily 2013-MCN-333 could potentially be an effective, safe, and tolerable treatment for moderate-to-severe melasma.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article