Merrimack在中期研究失败后停止开发实验性胰腺癌治疗药物

2018-06-26 MedSci MedSci原创

Merrimack制药公司在II期临床试验(CARRIE研究)中,实验性转移性胰腺癌治疗药物istiratumab(也被称为MM-141)未能达到其主要或次要临床终点。根据这些结果,Merrimack将不会投入更多资源来开发istiratumab。

Merrimack制药公司在II临床试验(CARRIE研究)中,实验性转移性胰腺癌治疗药物istiratumab(也被称为MM-141)未能达到其主要或次要临床终点。根据这些结果,Merrimack将不会投入更多资源来开发istiratumab

CARRIE研究涉及88例先前未经治疗的转移性胰腺癌和高血清游离胰岛素样生长因子-1水平的患者,这是大约50%的胰腺癌患者的普遍生物标志物。患者随机接受istiratumab或安慰剂治疗,联合纳他紫杉醇和吉西他滨。主要终点是无进展生存期,次要目标包括客观缓解率、疾病控制率、缓解持续时间、总体存活率和安全性

Merrimack指出,在所有分析的亚组中,istiratumab缺乏有效性的结论是一致的,CARRIE研究的完整数据将在未来的研究会议上提交。Merrimack首席执行官理查德·彼得斯表示:虽然这些结果令人失望,但我们的重点仍然放在另外两个实验性药物(MM-121MM-310)上,预计2018年将有数据得出。在SHERBOC试验中,MM-121(也被称为seribantumab),处于II期开发阶段,用于非小细胞肺癌患者以及转移性乳腺癌患者的治疗,而MM-310正在进行实体瘤患者的早期检测。


原始出处:

http://www.firstwordpharma.com/node/1574461#axzz5JX2NWGqk

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    2018-10-02 lujian
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    2018-10-18 yb6560
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    2019-01-21 surilei

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