海王生物晚间公告，公司全资子公司海王医药研究院研发的HW130注射液已于近日完成I期临床试验，并取得I期临床研究报告。此次临床试验为评价HW130治疗晚期恶性实体瘤患者的安全性、耐受性、药代动力学特征的剂量递增、开放的I期临床试验。HW130注射液I期临床试验达到了预期目的，为后续临床试验探索提供了充分依据。
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