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Alexion
adds fourth indication for
C5 inhibitor Ultomiris
C5
inhibitor Ultomiris in rare
autoimmune disorder
2024-03-25
·
EndPoints
上市批准
临床3期
临床结果
AstraZeneca
’s rare disease arm
Alexion
scored its fourth approval for
Ultomiris
in a
rare autoimmune disorder
after Phase 3 data showed there were zero patients with relapses over 73 weeks.
The FDA approved
Ultomiris
, the first and only long-acting
C5 complement inhibitor
C5 complement
inhibitor, for the treatment of adult patients with anti-
aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (NMOSD)
aquaporin-4
antibody-positive neuromyelitis optica spectrum disorder (NMOSD), a rare
autoimmune disease
that affects the central nervous system and can relapse unpredictably. Symptoms can include
blindness
and neurological problems that can lead to permanent disabilities.
Preview
来源: EndPoints
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文中所述内容并不反映新药情报库及其所属公司任何意见及观点,如有版权侵扰或错误之处,请及时联系我们,我们会在24小时内配合处理。
机构
Alexion Pharma Netherlands BV
AstraZeneca PLC
适应症
自身免疫性疾病
水通道蛋白4抗体阳性视神经脊髓炎谱系疾病
失明
靶点
C5
AQP4
药物
Ravulizumab-CWVZ
SAND-5 RGD
标准版
¥
16800
元/账号/年
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