欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tracleer
适用类别Human
治疗领域Scleroderma, Systemic;Hypertension, Pulmonary
通用名/非专利名称bosentan
活性成分bosentan (as monohydrate)
产品号EMEA/H/C/000401
患者安全信息No
许可状态Authorised
ATC编码C02KX01
是否额外监管Nei
是否仿制药或hybrid药物Nei
是否生物类似药Nei
是否附条件批准Nei
是否特殊情形Nei
是否加速审评Nei
是否罕用药Nei
上市许可日期2002/05/14
上市许可开发者/申请人/持有人Janssen-Cilag International N.V.  
人用药物治疗学分组Antihypertensives
兽用药物治疗学分组
审评意见日期2002/02/21
欧盟委员会决定日期2024/10/23
修订号45
治疗适应症Treatment of pulmonary arterial hypertension (PAH) to improve exercise capacity and symptoms in patients with WHO functional class III.Efficacy has been shown in: Primary (idiopathic and familial) PAH; PAH secondary to scleroderma without significant interstitial pulmonary disease; PAH associated with congenital systemic-to-pulmonary shunts and Eisenmenger's physiology. Some improvements have also been shown in patients with PAH WHO functional class II. Tracleer is also indicated to reduce the number of new digital ulcers in patients with systemic sclerosis and ongoing digital ulcer disease.
适用物种
兽用药物ATC编码
首次发布日期2017/11/20
最后更新日期2024/10/25
产品说明书https://www.ema.europa.eu/en/documents/product-information/tracleer-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tracleer
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