NL-OMON56009尚未招募3 期
A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel, Multicenter Study to Evaluate the Safety and Efficacy of ALXN1720 in Adults with Generalized Myasthenia Gravis. - ALXN1720-MG-301 (PREVAIL)
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 3
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Must be >= 18 years of age at the time of signing the informed consent
- •- Diagnosis of MG with generalized muscle weakness meeting the clinical
- •criteria defined by Myasthenia Gravis Foundation of America (MGFA) Class II,
- •- Positive serological test for autoantibodies against AChR.
排除标准
- •- History of thymectomy or any other thymic surgery within 12 months prior to
- •- Untreated thymic malignancy, carcinoma, or thymoma
- •- History of Neisseria meningitidis infection
- •- Pregnancy, breastfeeding, or intention to conceive during the course of the
研究者
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