海普瑞(002399.SZ)公告称，公司自主研发的创新候选药物注射用H1710已完成I期临床试验首例受试者入组及首次给药。H1710是一种低抗凝活性的肝素衍生物，是海普瑞自主研发的高效高选择性的乙酰肝素酶抑制剂。本次临床试验为开放、剂量递增的Ia期临床研究，计划在三家研究中心开展，预计入组约36名患者。H1710是以乙酰肝素酶为靶点治疗晚期实体瘤的创新药物，截至本公告日，于全球范围内尚无同一分子机制的同类产品上市。
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