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临床试验/NCT07643220
NCT07643220招募中1 期

An Open-Label, Randomized, Fasting, Single-Dose, Two-Sequence, Two-Period Crossover Study to Evaluate the Bioequivalence of "AJU-G721" and "G721R" in Healthy Adult Male Subjects

AJU Pharm Co., Ltd.1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2026年6月1日最近更新:
干预措施

试验速览

阶段
1 期
状态
招募中
入组人数
44
试验地点
1

研究概览

简要总结

To evaluate and compare the safety and pharmacokinetic profiles of "AJU-G721" (test drug) and "G721R" (reference drug) in healthy adult male subjects.

研究设计

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

入排标准

年龄范围
19 Years 至 54 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy male adults aged ≥19 years and <55 years at screening.
  • Body weight ≥ 50 kg and body mass index (BMI) between 18 and 30 kg/m².
  • Clinically healthy based on medical history, physical examination, ECG, and laboratory test results, as determined by the investigator.
  • Willing and able to provide written informed consent.
  • Agrees to use medically acceptable contraception during the required study period.

排除标准

  • Use of medications known to induce or inhibit drug-metabolizing enzymes within 30 days prior to the first dose, or other medications that may interfere with the study within 10 days prior to dosing.
  • Participation in another clinical trial involving an investigational product within 6 months prior to the first dose.
  • Whole blood donation within 8 weeks or component blood donation within 2 weeks prior to the first dose.
  • History of gastrointestinal resection that may affect drug absorption.
  • Known hypersensitivity to dutasteride, tamsulosin, or any component of the investigational product.
  • History of psychiatric illness, or any condition considered unsuitable for study participation by the investigator.

研究组 & 干预措施

Sequence A

Experimental

Period 1: Reference Drug, Single dose/ Period 2: Test Drug, Single dose

干预措施: Test Drug (Drug)

Sequence A

Experimental

Period 1: Reference Drug, Single dose/ Period 2: Test Drug, Single dose

干预措施: Reference Drug (Drug)

Sequence B

Experimental

Period 1: Test Drug, Single dose/ Period 2: Reference Drug, Single dose

干预措施: Test Drug (Drug)

Sequence B

Experimental

Period 1: Test Drug, Single dose/ Period 2: Reference Drug, Single dose

干预措施: Reference Drug (Drug)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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