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首页> 外文期刊>The Journal of dermatological treatment >The European Medicines Agency approval of 5-aminolaevulinic acid (Ameluz) for the treatment of actinic keratosis of mild to moderate intensity on the face and scalp: Summary of the scientific assessment of the Committee for Medicinal Products for Human Use
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The European Medicines Agency approval of 5-aminolaevulinic acid (Ameluz) for the treatment of actinic keratosis of mild to moderate intensity on the face and scalp: Summary of the scientific assessment of the Committee for Medicinal Products for Human Use

机译:欧洲药品管理局批准了5-氨基戊酸(Ameluz)用于治疗面部和头皮轻度至中度强度的光化性角化病:人类用药品委员会的科学评估摘要

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摘要

The European Commission has recently issued a marketing authorisation valid throughout the European Union for 5-aminolaevulinic acid (Ameluz). The decision was based on the favorable opinion of the CHMP recommending a marketing authorization for 5-aminolaevulinic acid for treatment of actinic keratosis of mild to moderate intensity on the face and scalp. The active substance is a sensitizer used in photodynamic/radiation therapy (ATC code L01XD04). The gel should cover the lesions and approximately 5 mm of the surrounding area with a film of about 1 mm thickness. The entire treatment area should be illuminated with a red light source, either with a narrow spectrum around 630 nm and a light dose of approximately 37 J/cm2 or a broader and continuous spectrum in the range between 570 and 670 nm with a light dose between 75 and 200 J/cm2. One session of photodynamic therapy should be administered for single or multiple lesions. Non- or partially responding lesions should be retreated in a second session 3 months after the first treatment. 5-aminolaevulinic acid is metabolized to protoporphyrin IX, a photoactive compound which accumulates intracellularly in the treated actinic keratosis lesions. Protoporphyrin IX is activated by illumination with red light of a suitable wavelength and energy. In the presence of oxygen, reactive oxygen species are formed which causes damage of cellular components and eventually destroys the target cells. The benefit with 5-aminolaevulinic acid is its ability to improve the complete response rate of actinic keratosis lesions. The most common side effects are reactions at the site of application. The objective of this article is to summarize the scientific review of the application. The detailed scientific assessment report and product information, including the summary of product characteristics (SmPC), are available on the EMA website (www.ema.europa.eu).
机译:欧盟委员会最近发布了在整个欧盟范围内有效的5-氨基戊酸(Ameluz)的销售授权。该决定基于CHMP的赞成意见,该建议推荐了5-氨基戊酸的销售许可,用于治疗面部和头皮的轻度到中度强度的光化性角化病。活性物质是光动力/放射疗法中使用的敏化剂(ATC代码L01XD04)。凝胶应覆盖病灶和周围约5 mm的周围区域,并形成厚度约1 mm的薄膜。整个治疗区域应使用红色光源照明,该光源应具有约630 nm的窄光谱和约37 J / cm2的光剂量,或具有570至670 nm范围内的较宽且连续的光谱,其光剂量介于75和200 J / cm2。对于单个或多个病变,应进行一期光动力疗法。在第一次治疗后3个月,应在第二次治疗中恢复无反应或部分反应的病变。 5-氨基松油酸被代谢成原卟啉IX,原卟啉IX在治疗的光化性角化病病变中在细胞内积累。原卟啉IX通过用适当波长和能量的红光照射来激活。在氧气的存在下,会形成活性氧,导致细胞成分受损并最终破坏靶细胞。 5-氨基松香酸的好处是它能够提高光化性角化病病变的完全缓解率。最常见的副作用是应用部位的反应。本文的目的是总结应用程序的科学综述。详细的科学评估报告和产品信息,包括产品特性摘要(SmPC),可在EMA网站(www.ema.europa.eu)上找到。

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