欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Holoclar
适用类别Human
治疗领域Stem Cell Transplantation;Corneal Diseases
通用名/非专利名称ex vivo expanded autologous human corneal epithelial cells containing stem cells
活性成分ex vivo expanded autologous human corneal epithelial cells containing stem cells
产品号EMEA/H/C/002450
患者安全信息No
许可状态Authorised
ATC编码S01XA19
是否额外监管Yes
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2015/02/17
上市许可开发者/申请人/持有人Holostem s.r.l.
人用药物治疗学分组Ophthalmologicals
兽用药物治疗学分组
审评意见日期2014/12/18
欧盟委员会决定日期2025/07/07
修订号13
治疗适应症Treatment of adult patients with moderate to severe limbal stem cell deficiency (defined by the presence of superficial corneal neovascularisation in at least two corneal quadrants, with central corneal involvement, and severely impaired visual acuity), unilateral or bilateral, due to physical or chemical ocular burns. A minimum of 1-2 mm2 of undamaged limbus is required for biopsy.
适用物种
兽用药物ATC编码
首次发布日期2017/06/22
最后更新日期2025/07/08
产品说明书https://www.ema.europa.eu/en/documents/product-information/holoclar-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/holoclar
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase