Efficacy and Tolerability of a New Facial 2-Mercaptonicotinoyl Glycine-Containing Depigmenting Serum Versus Hydroquinone 4% over 3-Month Treatment of Facial Melasma.

IF 3.5 3区 医学 Q1 DERMATOLOGY
Thierry Passeron, Delphine Kerob, Guénaëlle Le Dantec, Anne-Laure Demessant-Flavigny, Alessandro R do Nascimento, Renato Moura, Samir Salah, Mariana Feiges, Erika Fernandez, Andrew Alexis
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引用次数: 0

Abstract

Introduction: Topical treatment with hydroquinone 4% and hydroquinone-based preparations is the gold standard of care for melasma; however, it is limited by complications. 2-Mercaptonicotinoyl glycine (Melasyl™) is a new active ingredient targeting melanin synthesis without impairing the tyrosinase enzyme, with proven efficacy and safety. This study assessed the non-inferiority of a new facial depigmenting serum Mela B3® (MB3), containing 0.5% 2-mercaptonicotinoyl glycine, versus hydroquinone 4%.

Methods: This comparative, non-inferiority, randomized, investigator-blind, parallel-group investigation included adult women with mild-to-severe epidermal or mixed facial melasma. Patients received 3-month treatment with MB3 (twice daily) or hydroquinone 4% (once daily) and applied a broad spectrum SPF 50+/UVA tinted sunscreen (twice daily). Evaluations were conducted at day (D) 0, D28, D56, and D84 of treatment by a dermatologist and the patients. Non-inferiority analysis was performed at D84 on the Modified Melasma Area and Severity Index (mMASI) (non-inferiority margin 1.3). Efficacy assessments included mMASI, Melasma Quality of Life questionnaire (MELASQoL), and Patient Unique Stigmatization Holistic tool in Dermatology (PUSH-D) scores at each visit. Safety and tolerance were evaluated.

Results: The study included 109 women (phototypes I-IV; > 80% had phototypes III-IV). At D84, the estimated difference in mMASI score between MB3 and hydroquinone 4% was 0.46 (95% confidence interval - 0.25-1.17). Both groups demonstrated statistically significant improvements on mMASI from D28 versus baseline. The MELASQoL and PUSH-D scores decreased significantly from D28 in both groups (no difference between the groups). Nevertheless, a significant difference in the PUSH-D score was observed at D28 and D56 in favor of MB3. MB3 showed better tolerability versus hydroquinone 4% at D28 with fewer local skin reactions (6.0% versus 21.4%, respectively; p = 0.0286).

Conclusion: MB3 shows non-inferior efficacy and better tolerability compared with hydroquinone 4%. MB3 is an effective and well-tolerated alternative option for the topical treatment of melasma.

Clinical trial registration: NCT06787846.

一种新型面部2-巯基烟碱甘氨酸脱色血清与4%对苯二酚治疗面部黄褐斑3个月疗效和耐受性比较。
导论:4%对苯二酚和以对苯二酚为基础的制剂局部治疗是黄褐斑护理的金标准;然而,它受到并发症的限制。2-Mercaptonicotinoyl glycine (Melasyl™)是一种针对黑色素合成而不损害酪氨酸酶的新型活性成分,具有已证实的有效性和安全性。这项研究评估了一种新的面部脱色血清Mela B3®(MB3)的非劣效性,该血清含有0.5%的2-巯基烟碱甘氨酸,而对苯二酚含有4%。方法:这项比较、非劣效性、随机、研究者盲、平行组调查纳入了患有轻度至重度表皮或混合性面部黄褐斑的成年女性。患者接受为期3个月的MB3(每日两次)或对苯二酚4%(每日一次)治疗,并涂抹广谱SPF 50+/UVA着色防晒霜(每日两次)。由皮肤科医生和患者在治疗的第0天、第28天、第56天和第84天进行评估。改良黄褐斑面积和严重程度指数(mMASI)在D84时进行非劣效性分析(非劣效度为1.3)。疗效评估包括每次就诊时的mMASI、黄褐斑生活质量问卷(MELASQoL)和患者独特污名化皮肤科整体工具(PUSH-D)评分。评估了安全性和耐受性。结果:研究纳入109名女性(照片型I-IV;> 80%为III-IV型)。在D84时,MB3和对苯二酚4%之间的mMASI评分估计差异为0.46(95%置信区间- 0.25-1.17)。与基线相比,两组的mMASI均有统计学上的显著改善。两组患者的MELASQoL和PUSH-D评分均较D28显著下降(组间无差异)。然而,在D28和D56时观察到PUSH-D评分有显著差异,有利于MB3。与对苯二酚相比,MB3在D28时表现出更好的耐受性4%,局部皮肤反应较少(分别为6.0%和21.4%;p = 0.0286)。结论:与对苯二酚相比,MB3疗效不差,耐受性好4%。MB3是一种有效且耐受性良好的黄褐斑局部治疗替代方案。临床试验注册:NCT06787846。
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来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an International and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
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