首页> 外文期刊>Journal of drugs in dermatology: JDD >Clinical Efficacy and Safety of a Multimodality Skin Brightener Composition Compared With 4% Hydroquinone
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Clinical Efficacy and Safety of a Multimodality Skin Brightener Composition Compared With 4% Hydroquinone

机译:与4%对苯二酚相比,多峰型皮肤增白剂组合物的临床疗效和安全性

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摘要

There are numerous common skin disorders involving hyperpigmentation, including solar lentigines, postinflammatory hyperpigmenta-tion, melasma, freckles, and dyschromia from photoaging. While these conditions are of an aesthetic nature, there is great interest in newer, safer, and more effective treatment modalities. Topical hydroquinone (HQ) has been the gold standard of skin lighteners for many years. However, regulatory authorities around the world are now questioning its safety. A randomized, double-blind, half-face study was conducted in females having moderate to severe facial hyperpigmentation to assess the efficacy and tolerability of 3 new skin brightener formulations containing SMA-432, a prostaglandin E2 inhibitor, compared with 4% HQ, Each subject was assigned 2 of the 4 test materials and was instructed to apply the product on the assigned side of the face twice daily for 12 weeks. Evaluation visits were conducted at baseline and at 4, 8, and 12 weeks. At each visit, subjects were evaluated by a blinded investigator for clinical efficacy and tolerability using grading scales. Standardized digital photography and Chroma Meter assessments were also taken. Self-assessment questionnaires were completed at weeks 4, 8, and 12. Sixty-eight Caucasian subjects (136 half faces) completed the study. All test materials significantly reduced Overall Hyperpigmentation and improved the Investigator's Global Hyperpigmentation Improvement rating at weeks 4, 8, and 12 compared with baseline. SMA-432 exhibited a dose-dependent improvement in hyperpigmentation. There were no major tolerability issues with any of the test materials. Self-assessments were generally favorable for all test materials. At the completion of the trial, subjects rated one of the tested multimodality brightener compositions as the most favorable product and 4% HQ as the least favorable. This study demonstrated that the new non-HQ-containing skin brightener formulations were as effective and equally well tolerated as the gold standard, 4% HQ, in females with facial hyperpigmentation.
机译:有许多涉及色素沉着过度的常见皮肤疾病,包括日光性角质素,炎症后色素沉着过度,黄褐斑,雀斑和光老化引起的色素减退。虽然这些条件具有美学性质,但人们对更新,更安全和更有效的治疗方式非常感兴趣。多年来,局部对苯二酚(HQ)已成为亮肤剂的金标准。但是,世界各地的监管机构现在都在质疑其安全性。对患有中度至重度色素沉着过度的女性进行了一项随机,双盲,半脸研究,以评估含有前列腺素E2抑制剂SMA-432(与4%的HQ相比)的3种新皮肤增白剂的功效和耐受性受试者被分配了4种测试材料中的2种,并被指示每天两次在面部指定的一侧涂抹产品,持续12周。在基线以及第4、8和12周进行评估访问。每次访视时,由盲人研究者使用分级量表对受试者的临床疗效和耐受性进行评估。还进行了标准化的数字摄影和色度仪评估。在第4、8和12周完成了自我评估问卷。68名白人受试者(136个半脸)完成了研究。与基线相比,所有测试材料在第4、8和12周时均显着减少了总体色素沉着的增加,并提高了研究者的总体色素沉着改善等级。 SMA-432在色素沉着方面表现出剂量依赖性的改善。任何测试材料都没有重大的公差问题。自我评估通常适用于所有测试材料。在试验完成时,受试者将一种测试的多峰性增白剂组合物评为最佳产品,将4%的HQ评为最低产品。这项研究表明,在面部色素沉着过度的女性中,新的不含HQ的皮肤增白剂配方与黄金标准4%HQ一样有效,并且具有相同的耐受性。

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