跳至主要内容
临床试验/2025-523950-15-01
2025-523950-15-01招募中2 期

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study With a Long-term Extension of Povetacicept in Adults with Generalized Myasthenia Gravis

Vertex Pharmaceuticals Inc.7 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2026年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
5
试验地点
7
主要终点
Phase 2: Percent change in total immunoglobulin G (IgG) [Time Frame: Baseline and At Week 12]

研究概览

简要总结

Phase 2: To evaluate the PD effect of povetacicept in subjects with gMG, Phase 2 and LTE: To evaluate the safety and tolerability of povetacicept in subjects with gMG

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Age ≥18 years
  • Diagnosis of generalized myasthenia gravis with generalized muscle weakness and fitting MGFA clinical classification II-IV
  • Additional inclusion criteria are defined in the protocol

排除标准

  • History of thymic surgery within 6 months of screening
  • History of malignancy within the last 5 years
  • Additional exclusion criteria are defined in the protocol

研究组 & 干预措施

ALPN-303 solution for injection in pre-filled syringe

Test

干预措施: ALPN-303 solution for injection in pre-filled syringe (Drug)

Test IMP without active substance

Placebo

干预措施: Test IMP without active substance (Drug)

结局指标

主要结局

Phase 2: Percent change in total immunoglobulin G (IgG) [Time Frame: Baseline and At Week 12]

Phase 2: Percent change in total immunoglobulin G (IgG) [Time Frame: Baseline and At Week 12]

Phase 2 and LTE: Safety and tolerability as Assessed by Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)

Phase 2 and LTE: Safety and tolerability as Assessed by Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)

次要结局

未报告次要终点

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Clinical Trials and Medical Info

Scientific

Vertex Pharmaceuticals Inc.

研究点 (7)

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