【新诺威:SYS6041抗体偶联药物获美国临床试验批准】新诺威公告,控股子公司巨石生物申报的SYS6041注射剂临床试验申请已获得美国FDA批准,可以在美国开展临床试验。该药物是一款单克隆抗体偶联药物,适用于晚期实体瘤,已在国内外提交多件专利申请。此前,该产品已于2025年1月获得中国国家药品监督管理局批准,可以在中国开展临床试验。

金融界
14 Apr
新诺威公告,控股子公司巨石生物申报的SYS6041注射剂临床试验申请已获得美国FDA批准,可以在美国开展临床试验。该药物是一款单克隆抗体偶联药物,适用于晚期实体瘤,已在国内外提交多件专利申请。此前,该产品已于2025年1月获得中国国家药品监督管理局批准,可以在中国开展临床试验。

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