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创新药HSK21542注射液获批开展 “肝病瘙痒”的Ⅱ期临床试验
2021-08-03 11:55:28
2021年7月，海思科全资子公司辽宁海思科制药有限公司获得国家药品监督管理局药品审评中心下发的《药物临床试验批准通知书》，获批开展“肝病瘙痒”的Ⅱ期临床试验。
HSK21542已经完成两项健康人I期临床试验，其他已经申请的IND包括两个适应症分别为急慢性疼痛（PhaseⅢ进行中）及瘙痒适应症（PhaseⅡ进行中）。
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