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A Randomized, Multicenter, Evaluator-blind Study to Evaluate the Safety and Effectiveness of VYC-12L Treatment for Skin Quality Improvements.
Alexiades, Macrene; Palm, Melanie D; Kaufman-Janette, Joely; Papel, Ira; Cross, Sarah J; Abrams, Steve; Chawla, Smita.
Afiliação
  • Alexiades M; Associate Clinical Professor, School of Medicine, Yale University, New Haven, Connecticut.
  • Palm MD; Dermatology & Laser Surgery Center of New York, New York.
  • Kaufman-Janette J; Art of Skin MD, Solana Beach, California.
  • Papel I; Skin Associates of South Florida, Coral Gables, Florida.
  • Cross SJ; Division of Facial Plastic and Reconstructive Surgery, Department of Otolaryngology - Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Abrams S; AbbVie Inc, Irvine, California.
  • Chawla S; AbbVie Inc, Irvine, California.
Dermatol Surg ; 49(7): 682-688, 2023 07 01.
Article em En | MEDLINE | ID: mdl-37163665
ABSTRACT

BACKGROUND:

Skin quality may be assessed by degrees of skin smoothness, fine lines, and hydration. VYC-12L is a recently developed hyaluronic acid filler to improve skin quality.

OBJECTIVE:

This was a randomized, evaluator-blind study assessing safety and effectiveness of intradermal VYC-12L treatment for improving cheek skin smoothness, fine lines, and hydration.

METHODS:

Participants (≥22 years) with moderate-to-severe investigator-assessed Allergan Cheek Smoothness Scale (ACSS) scores were randomized in 21 ratio to receive VYC-12L or control (no treatment with optional treatment). Effectiveness was assessed 1 month after last injection (initial or touch-up) by a responder rate (≥1-grade improvement from baseline on both cheeks) using investigator-rated ACSS and Allergan Fine Lines Scale (AFLS), and tissue dielectric constant probe-measured skin hydration. Safety was evaluated throughout.

RESULTS:

Participants (VYC-12L, n = 131; control, n = 71) were 86.1% female with a median age of 58.0 years. At month 1, ACSS and AFLS responder rates were statistically significantly higher in the VYC-12L group (57.9%, 58.3%, respectively) than in the untreated controls (4.5%, 5.4%, respectively; p < .001). VYC-12L ACSS and AFLS responder rates remained consistent throughout the 6-month follow-up. Six participants reported treatment-related adverse events; none led to study discontinuation.

CONCLUSION:

VYC-12L is an effective, well-tolerated treatment for lasting improvement of cheek skin smoothness, fine lines, and hydration.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento da Pele / Técnicas Cosméticas / Preenchedores Dérmicos Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Dermatol Surg Assunto da revista: DERMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Envelhecimento da Pele / Técnicas Cosméticas / Preenchedores Dérmicos Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Dermatol Surg Assunto da revista: DERMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article