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相关临床试验
28
17 进行中
药物批准
0
批准总数
监管机构
监管机构数
成立时间
1998
进行中(未招募)
17
60.7%
已完成
9
32.1%
终止
1
3.6%
撤回
暂无批准数据
- NovelMed's Ruxoprubart demonstrated significant efficacy in a Phase II trial for treatment-naïve PNH patients, meeting all primary endpoints including complete transfusion avoidance and increased hemoglobin levels. - The drug's selective inhibition of the Alternative Pathway without affecting the Classical Pathway offers a potentially safer profile than existing treatments, which often carry Black Box warnings for infection risk. - With FDA Orphan Drug Designation already secured and plans to file for Breakthrough Therapy Designation, Ruxoprubart is positioned as a potential best-in-class therapy for PNH and other complement-mediated disorders.