跳至主要内容
临床试验/NCT05110118
NCT05110118已完成1 期

A Randomized, Double-blind, Single-dose, Parallel-group Study Comparing Pharmacokinetic Characteristics, Safety , Tolerability and Immunogenicity of LY01008 (Recombinant Humanized Anti-Human Vascular Endothelial Growth Factor Monoclonal Antibody Injection) and Avastin (Bevacizumab Injection) in Healthy Chinese Male Subjects

Shandong Boan Biotechnology Co., Ltd1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2020年8月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
112
试验地点
1
主要终点
Terminal elimination half-life(t1/2)

研究概览

简要总结

This is a randomized, double-blind, single-dose, parallel-group study comparing pharmacokinetic characteristics, safety , tolerability and immunogenicity of LY01008 (Recombinant Humanized Anti-Human Vascular Endothelial Growth Factor Monoclonal Antibody Injection) and Avastin (Bevacizumab Injection) in healthy Chinese male subjects.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy male volunteers
  • Subjects aged 18 - 45 years
  • Subjects weighing ≥ 50.0 kg and ≤ 100.0 kg
  • Subjects with a body mass index (BMI) ≥ 19.0 and ≤ 26.0 kg/m2

排除标准

  • Subjects with evidence or history of clinically significant disease
  • Subjects with a history of previous cancer
  • Subjects with a history of hypertension, or abnormal blood pressure at screening/baseline measurements (systolic blood pressure > 140 mmHg and/or diastolic blood pressure > 90 mmHg confirmed by a repeat measurement on the same day)
  • Subjects with a history of blood donation 3 months before study drug infusion
  • Subjects with a history of exposure to antibodies 12 months before study drug infusion
  • Subjects with previous exposure to anti-VEGF therapy

研究组 & 干预措施

LY01008

Experimental

Single intravenous injection of LY01008 3 mg/kg for 90 min(±1 min).

干预措施: LY01008 (Drug)

Avastin

Active Comparator

Single intravenous injection of Avastin 3 mg/kg for 90 min(±1 min).

干预措施: Avastin (Drug)

结局指标

主要结局

Terminal elimination half-life(t1/2)

时间窗: From baseline to Day 99

Apparent volume of distribution(Vd)

时间窗: From baseline to Day 99

Maximum (peak) plasma concentration(Cmax)

时间窗: From baseline to Day 99

Area under the plasma concentration-time curve from time zero to infinity(AUC0-∞)

时间窗: From baseline to Day 99

Area under the plasma concentration-time curve from time zero to the last measurable concentration(AUC0-t)

时间窗: From baseline to Day 99

Chloride(CL)

时间窗: From baseline to Day 99

次要结局

  • Vital signs(From baseline to Day 99)
  • Clinical laboratory tests(From baseline to Day 99)
  • Positive rate of neutralizing antibody (NAb)(From baseline to Day 99)
  • Adverse Events(AEs)(From baseline to Day 99)
  • Physical examinations(From baseline to Day 99)
  • 12-lead ECGs(From baseline to Day 99)
  • Positive rate of serum anti-drug antibody (ADA)(From baseline to Day 99)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Pharmacokinetic Characteristics, Safety,... | 临床试验