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Safety and efficacy of a carboxymethyl chitosan dermal injection device for the treatment of skin defects: a first-in-man, pilot, comparative, split-body study.
Philippart, Catherine; Hendrickx, Benoit; Rharbaoui, Siham; Natalizio, Audrey; Boisnic, Sylvie; Micheels, Patrick; Gautier, Sandrine; Douette, Pierre; Hermitte, Laurence.
Afiliação
  • Philippart C; KiOmed Pharma; Rue Haute Claire 4; 4040 Herstal, Belgium.
  • Hendrickx B; University Hospital Brussels (UZB), Laarbeeklaan 101, 1090 Jette, Belgium.
  • Rharbaoui S; Eurofins-Dermscan; 114 Boulevard du 11 novembre 1918; 69100 Villeurbanne, France.
  • Natalizio A; Eurofins-Dermscan; 114 Boulevard du 11 novembre 1918; 69100 Villeurbanne, France.
  • Boisnic S; Gredeco; 45 Boulevard Auriol; 75013 Paris, France.
  • Micheels P; Private practice, Geneva, Switzerland.
  • Gautier S; KiOmed Pharma; Rue Haute Claire 4; 4040 Herstal, Belgium.
  • Douette P; Full-time consultant for KiOmed Pharma at the time of the study.
  • Hermitte L; KiOmed Pharma; Rue Haute Claire 4; 4040 Herstal, Belgium.
Eur J Dermatol ; 2021 Aug 26.
Article em En | MEDLINE | ID: mdl-34463288
ABSTRACT
Injectable soft-tissue devices are increasingly used for improving skin defects and deficiencies related to ageing. To assess the safety and efficacy of KIO015, a new injectable soft-tissue device formulated with carboxymethyl chitosan for the intradermal treatment of skin defects associated with ageing. Twenty-two subjects (40-65 years) were randomized to receive injections in the neckline of KIO015 and a non-cross-linked HA-based device, and were followed for up to 10 months. Injection site reactions (ISRs) and adverse events (AEs) were documented. Skin improvement was assessed instrumentally and clinically. Skin biopsies at injection zones in the lower back were taken at Day 28 for histopathology and immunohistochemistry analyses, to further assess product performance. Histomorphometric analyses on rabbits and in vitro assessment of KIO015 antioxidant capacity were also conducted. KIO015 was very well tolerated. Only expected and transient ISRs were observed; mainly erythema and hematoma. No adverse local effects or foreign body granuloma were observed histologically. Both clinical and instrumental evaluations confirmed the performance of KIO015. The skin was firmer and more elastic. Skin hydration showed significant improvement three days after injection. KIO015 exhibited superior overall maintenance of skin hydration after 10 months as compared to HA. These clinical results were supported by in vitro trials and implantation tests in the rabbit. The results from this pilot study support the use of KIO015 as an innovative alternative to HA-based devices for intradermal treatment of skin disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2021 Tipo de documento: Article