【宜明昂科-B(01541.HK)获国家药监局批准进行替达派西普联合珀维拉芙普α另加化疗或不加化疗用于治疗晚期恶性肿瘤的临床试验】宜明昂科-B(01541.HK)发布公告,集团已获中华人民共和国国家药品监督管理局(国家药监局)批准进行IMM01(替达派西普)联合IMM2510(珀维拉芙普α),另加化疗或不加化疗用于治疗晚期恶性肿瘤的临床试验。这一重大进展标志着公司在快速推进IMM01(替达派西普)及IMM2510(珀维拉芙普α)的临床研究方面又迈出了关键一步。

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宜明昂科-B(01541.HK)发布公告,集团已获中华人民共和国国家药品监督管理局(国家药监局)批准进行IMM01(替达派西普)联合IMM2510(珀维拉芙普α),另加化疗或不加化疗用于治疗晚期恶性肿瘤的临床试验。这一重大进展标志着公司在快速推进IMM01(替达派西普)及IMM2510(珀维拉芙普α)的临床研究方面又迈出了关键一步。

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