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临床试验/NCT02326233
NCT02326233已完成1 期

A Randomised, Open-labelled, Two-arm, Parallel Group, Single-dose Study to Compare the Pharmacokinetics, Safety, and Tolerability of the Pre-filled Pen and PFS of SB5 in Healthy Subjects

Samsung Bioepis Co., Ltd.2 个研究点 分布在 2 个国家目标入组 190 人开始时间: 2015年6月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
190
试验地点
2
主要终点
Area Under the Concentration-time Curve From Time Zero to the Last Quantifiable Concentration (AUClast)

研究概览

简要总结

The purpose of this study is to compare the pharmacokinetics, safety, and tolerability of the pre-filled pen and pre-filled syringe of SB5 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

  • Healthy subjects
  • Have a body mass index between 20.0 to 29.9 kg/m², inclusive.

排除标准

  • History and/or current presence of clinical significant atopic allergy, hypersensitivity or allergic reactions, also including known or suspected clinically relevant drug hypersensitivity to any components of the test and reference investigational product formulation or comparable drugs
  • Active or latent Tuberculosis or who have a history of Tuberculosis
  • History of invasive systemic fungal infections or other opportunistic infections
  • Systemic or local infection, a known risk for developing sepsis and/or known active inflammatory process
  • Serious infection associated with hospitalisation and/or which required intravenous antibiotics
  • History of and/or current cardiac disease
  • Have received live vaccine(s) within 4 weeks prior to Screening or who will require live vaccine(s) between Screening and the subject's last visit
  • Intake medication with a half-life > 24 h within 4 weeks or 10 half-lives of the medication prior to investigational product administration

研究组 & 干预措施

Pen of SB5

Experimental

Pen of SB5, single-dose of 40 mg via subcutaneous injection (study drug)

干预措施: Pen of SB5 (Biological)

PFS of SB5

Active Comparator

PFS of SB5, single-dose of 40 mg via subcutaneous injection (reference drug)

干预措施: PFS of SB5 (Biological)

结局指标

主要结局

Area Under the Concentration-time Curve From Time Zero to the Last Quantifiable Concentration (AUClast)

时间窗: 0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose

Maximum Serum Concentration (Cmax)

时间窗: 0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose

Area Under the Concentration-time Curve From Time Zero to Infinity (AUCinf)

时间窗: 0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose

次要结局

  • Time to Reach Cmax (Tmax)(0, 24, 48, 96, 120, 144, 168, 216, 264, 336, 408, 504, 600, 696, 840, 1008, and 1344 h postdose)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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