华东医药公告，公司全资子公司中美华东收到国家药品监督管理局的《药物临床试验批准通知书》，批准其申报的注射用HDM2020进行临床试验。HDM2020是一种靶向成纤维细胞生长因子受体2b的新型抗体药物偶联物，旨在治疗晚期实体瘤。该药物在临床前研究中显示出显著的抗肿瘤活性。此次临床试验批准是HDM2020研发的重要里程碑，将提升公司在肿瘤治疗领域的竞争力。华东医药将继续推进药物研发，并根据进展及时披露信息。
华东医药公告，公司全资子公司中美华东收到国家药品监督管理局的《药物临床试验批准通知书》，批准其申报的注射用HDM2020进行临床试验。HDM2020是一种靶向成纤维细胞生长因子受体2b的新型抗体药物偶联物，旨在治疗晚期实体瘤。该药物在临床前研究中显示出显著的抗肿瘤活性。此次临床试验批准是HDM2020研发的重要里程碑，将提升公司在肿瘤治疗领域的竞争力。华东医药将继续推进药物研发，并根据进展及时披露信息。
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