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临床试验/NCT02564497
NCT02564497已完成1 期

A Randomized, Open-label, Parallel-group, Single-dose, Biocomparability Study of the Pharmacokinetics of Belatacept Drug Products Using Active Pharmaceutical Ingredient Manufactured by Process E Relative to Active Pharmaceutical Ingredient Manufactured by Process C in Healthy Subjects

Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 491 人开始时间: 2015年10月2日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
491
试验地点
1
主要终点
Maximum Observed Serum Concentration (Cmax) of Belatacept

研究概览

简要总结

The purpose of the study is to compare the Pharmacokinetics (PK) of Process E belatacept relative to Process C belatacept in Healthy subjects

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Signed Informed Consent
  • Target population: Healthy males and females.
  • Males and females, ages 18 to 55 years, inclusive.
  • Women of child bearing potential (WOCBP) with negative serum or urine pregnancy test
  • Women must not be breastfeeding
  • Men and WOCBP must agree to follow instructions for contraception

排除标准

  • History of TB, malignancy, any other chronic or acute infecton or disease.
  • History of acute or chronic medical illness
  • Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG or clinical laboratory determinations beyond what is consistent with the target population.
  • History of allergy to belatacept or related compounds -

研究组 & 干预措施

Process E Belatacept

Other

Active Pharmaceutical Ingredient (API) of Belatacept manufactured by Process E

干预措施: Process E Belatacept (Biological)

Process C Belatacept

Other

Active Pharmaceutical Ingredient (API) of Belatacept manufactured by Process C

干预措施: Process C Belatacept (Biological)

结局指标

主要结局

Maximum Observed Serum Concentration (Cmax) of Belatacept

时间窗: Day 1 to Day 71

Cmax was derived from serum concentration versus time data. Serum samples were analyzed for belatacept by a validated enzyme-linked immunosorbent assay (ELISA). Cmax was measured in nanograms per milliliter.

Area Under the Serum Concentration-time Curve From Time Zero Extrapolated to Infinite Time (INF) of Belatacept.

时间窗: Day 1 to Day 71

(AUC\[INF\]) was derived from serum concentration versus time data and measured in nanogram hours per milliliter (ng\*h/mL). Serum samples were analyzed for belatacept by a validated enzyme-linked immunosorbent assay (ELISA)

次要结局

  • Area Under the Serum Concentration-time Curve From Time Zero to Time of the Last Quantifiable Concentration (AUC 0-T)(Day 1 to Day 71)
  • Half Life (T-HALF)(Day 1 to Day 71)
  • Time of Maximum Observed Serum Concentration (Tmax)(Day 1 to Day 71)
  • Total Body Clearance (CLT)(Day 1 to Day 71)
  • Volume of Distribution at Steady State (Vss)(Day 1 to Day 71)

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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