跳至主要内容
临床试验/2023-509399-40-00
2023-509399-40-00
已完成
1 期

AN OPEN-LABEL, RANDOMIZED, SINGLE DOSE, TWO-STAGE CROSSOVER ADAPTIVE BIOEQUIVALENCE STUDY OF TRIAMCINOLONE ACETONIDE 40 MG/ML STERILE INJECTABLE SUSPENSION (Test product–Lisapharma S.p.A) VERSUS KENACORT® 40 MG/ML SUSPENSION (Reference product – Bristol Myers Squibb) AFTER INTRAMUSCULAR ADMINISTRATION TO HEALTHY VOLUNTEERS

Laboratorio Italiano Biochimico Farmaceutico Lisapharma S.p.A.1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年4月4日最近更新:

概览

阶段
1 期
状态
已完成
入组人数
30
试验地点
1

概览

简要总结

暂无简介。

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

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

Matteo Farina

Scientific

Laboratorio Italiano Biochimico Farmaceutico Lisapharma S.p.A.

研究点 (1)

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