信达生物(01801.HK)宫颈癌联合疗法二期临床研究完成首例患者给药
信达生物(01801.HK)公布,联合疗法用於治疗二线及以上晚期宫颈癌的第二期关键临床研究,已完成首例患者入组及给药。
该研究在中国开展,用於评估抗CTLA-4单克隆抗体IBI310联合信迪利单抗注射液「达伯舒」,对经一线及以上含铂化疗失败的晚期宫颈癌的有效性和安全性。信达生物医学科学与战略肿瘤部副总裁周辉表示,前期临床研究结果显示IBI310联合达伯舒具有良好的安全性和抗肿瘤活性。
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