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临床试验/NCT06155955
NCT06155955招募中2 期

Comparison of Outcomes Between Low Dose Emicizumab and Extended Half-life Factor VIII With Pharmacokinetic-guided Prophylaxis in Clinically Severe Hemophilia A

Chulalongkorn University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2023年6月22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
15
试验地点
1
主要终点
treated spontaneous bleeds, treated joint bleeds

研究概览

简要总结

  • To outcome between low dose Emicizumab and low dose prophylaxis with FVIII concentration
  • To study pharmacokinetic, side effect of low dose Emicizumab

详细描述

  • To compare outcome between low dose Emicizumab and low dose prophylaxis with FVIII concentration using ABR, AJBR and HJHS, HaemoQoL
  • To study pharmacokinetic, side effect and effectiveness of low dose Emicizumab

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
3 Years 至 30 Years(Child, Adult)
性别
Male
接受健康志愿者

入选标准

  • Severe or moderate Hemophilia A with baseline FVIII:C of <3 IU/dl or severe bleeding phenotype
  • Receiving low dose FVIII prophylaxis for at least 6 months

排除标准

  • Detectable FVIII inhibitor at screening
  • Detectable FVIII inhibitor at screening Having other underlying diseases: Juvenile rheumatoid arthritis, metabolic bone diseases, or other conditions mimicking or causing joint diseases

研究组 & 干预措施

low dose emicizumab

Experimental

2 mg per kilograms per dose in first month, loading every 2 weeks then every 4 weeks

干预措施: "Emicizumab", "HEMLIBRA®" (Drug)

结局指标

主要结局

treated spontaneous bleeds, treated joint bleeds

时间窗: 6 months after start low dose emicizumab as secondary prophylaxis treatment

Using "Annualized joint bleeding rate" (AJBR)

spontaneous and traumatic bleeding rate

时间窗: 6 months after start low dose emicizumab as secondary prophylaxis treatment

Using "Annualized bleeding rate" (ABR)

The function of the knee, elbow, and ankle joints

时间窗: 6 months after start low dose emicizumab as secondary prophylaxis treatment

Using "Hemophilia Joint Health Score" (HJHS)

次要结局

未报告次要终点

研究者

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

Nuchanun Kessakorn, MD

MD

Chulalongkorn University

研究点 (1)

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