智通财经APP讯，康弘药业(002773.SZ)发布公告，近日，公司子公司四川弘合生物科技有限公司(以下简称“弘合生物”)收到国家药品监督管理局签发的注射用KH617《药物临床试验批准通知书》，该药品适应症：与标准治疗方案联合治疗新诊断的胶质母细胞瘤。
注射用KH617是弘合生物合成生物学平台首个进入临床试验的产品，属于化药1类创新药，I期临床研究显示，注射用KH617安全性和耐受性良好，且已初步观察到抗肿瘤的积极疗效信号，有望为胶质母细胞瘤患者提供新的治疗方案。
智通财经APP讯，康弘药业(002773.SZ)发布公告，近日，公司子公司四川弘合生物科技有限公司(以下简称“弘合生物”)收到国家药品监督管理局签发的注射用KH617《药物临床试验批准通知书》，该药品适应症：与标准治疗方案联合治疗新诊断的胶质母细胞瘤。
注射用KH617是弘合生物合成生物学平台首个进入临床试验的产品，属于化药1类创新药，I期临床研究显示，注射用KH617安全性和耐受性良好，且已初步观察到抗肿瘤的积极疗效信号，有望为胶质母细胞瘤患者提供新的治疗方案。
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