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临床试验/NCT06968338
NCT06968338招募中1 期

A Phase 1, Randomized, Double-Blinded, Placebo-Controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Single and Multiple Ascending Doses of ARGX-213 in Healthy Adult Participants

argenx1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年4月11日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
发起方
argenx
入组人数
80
试验地点
1
主要终点
Incidence of adverse events, serious adverse events, and adverse events leading to the discontinuation

研究概览

简要总结

This study aims to assess the safety of ARGX-213 in healthy adults. Another aim is to measure the amount of ARGX-213 in the blood over time to learn how it moves through the body and acts in the body. The participants will remain in the study for approximately up to 21 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Is at least the local legal age of consent for clinical studies and is aged 18 to 65 years, inclusive, when signing the ICF
  • Is a female of nonchild bearing potential (either postmenopausal or surgically sterilized) or a male
  • Has a body weight between 50 and 100 kg and a BMI between 18 and 30.5 kg/m^2, inclusive

排除标准

  • Has any current or past clinically meaningful medical or psychiatric condition that, in the investigator's opinion, would confound the results of the study or put the participant at undue risk
  • Has a clinically meaningful abnormality detected on ECG recording regarding either rhythm or conduction

研究组 & 干预措施

ARGX-213

Experimental

Participants receiving the experimental drug

干预措施: ARGX-213 (Biological)

Placebo

Placebo Comparator

Participants receiving placebo

干预措施: Placebo (Other)

结局指标

主要结局

Incidence of adverse events, serious adverse events, and adverse events leading to the discontinuation

时间窗: Up to 17 weeks

次要结局

  • ARGX-213 serum concentrations(Up to 17 weeks)
  • Percent change from baseline in total IgG concentrations in serum(Up to 17 weeks)
  • Incidence of antidrug antibodies against ARGX-213 in serum(Up to 17 weeks)

研究者

发起方
argenx
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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