欧盟批准血小板减少症药物Doptelet

2020-11-06 MedSci原创 MedSci原创

Doptelet通过模拟血小板生成素刺激巨核细胞发育和成熟,增加血小板数量。

Sobi公司的血小板生成素受体(TPO-R)激动剂Doptelet(avatrombopag),在欧盟获批用于治疗成人慢性肝病(CLD)患者的严重血小板减少症。

血小板减少症的特征是血液中血小板数量减少,这是CLD患者常见的并发症。随着肝脏疾病病变更加严重,血小板减少症的程度通常也会恶化。Doptelet是通过模拟血小板生成素刺激巨核细胞发育和成熟的生物学作用,增加血小板数量。

Avotrombopag Illustration by Jackie Heda | Medical Illustration & Animation

在两项ADAPT-1和ADAPT-2 III期临床试验中,Doptelet在患有严重血小板减少症的CLD患者中进行治疗时,可有效增加血小板数量和减少血小板输注治疗。

Doptelet先前也获得了美国食品和药物管理局(FDA)的批准,用于治疗CLD成年患者的血小板减少症。

原始出处:

http://www.pharmatimes.com/news/sobi_launches_thrombocytopenia_med_doptelet_in_eu_1355930

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    2020-11-08 noboaty

    重肝患者的福利

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    2020-11-08 cy0329
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