Immunome Inc.今日宣布，其候选药物IM-1340已获得美国食品药品监督管理局（FDA）的临床试验申请（IND）许可。IM-1340是一款潜在的first-in-class抗体偶联药物（ADC），拟用于实体瘤的治疗。
Immunome Inc.今日宣布，其候选药物IM-1340已获得美国食品药品监督管理局（FDA）的临床试验申请（IND）许可。IM-1340是一款潜在的first-in-class抗体偶联药物（ADC），拟用于实体瘤的治疗。
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