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临床试验/NCT02781753
NCT02781753已完成1 期

A Phase 1 Study to Evaluate the Pharmacokinetic and Pharmacodynamic Profile, Safety, and Tolerability of Escalating Single Dose Recombinant Human Serum Albumin/Interferon alpha2b Fusion Protein in Healthy Chinese Volunteers

Tianjin SinoBiotech Ltd.1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2016年4月7日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
Number of participants with adverse events after single dose

研究概览

简要总结

The purpose of this study is to evaluate the dosages of recombinant human serum albumin/interferon alpha2b fusion protein injection in healthy subjects.

详细描述

This is an open-label study that will be conducted at a single site in China to characterize the PK/PD profile, safety and tolerability of Recombinant Human Serum Albumin/interferon alpha2b Fusion Protein in healthy subjects. Subjects will receive a single dose of Recombinant Human Serum Albumin/interferon alpha2b Fusion Protein or active comparator Pegasys at Day 0. The total duration of study participation is up to 6 weeks for each subject. Subjects will complete a follow-up visit at Day 28 after the dosing.

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
None

入排标准

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

入选标准

  • Must be healthy males or females between 18 to 45 years old, inclusive
  • Must have a body mass index (BMI) of 19 to 25 kg/m2, inclusive, and a minimum body weight of 50.0 kg

排除标准

  • History of any clinically significant laboratory abnormalities, cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal, or other major diseases
  • Female subjects who are pregnant or breastfeeding
  • Any previous treatment with Human Albumin Interferon fusion protein

结局指标

主要结局

Number of participants with adverse events after single dose

时间窗: 4 weeks

Frequency and severity of all adverse events on the part of the participants, including frequency and severity of drug-related adverse events.

次要结局

  • Plasma concentration of Neopterin after single dose(4 weeks)
  • Pharmacokinetics of interferon after single dose(4 weeks)

研究者

发起方
Tianjin SinoBiotech Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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