跳至主要内容
临床试验/NCT07364851
NCT07364851尚未招募1 期

A Randomized, Open-label, Single-dose, 2-sequence, Two-period, Crossover Phase 1 Clinical Trial to Evaluate the Safety and Pharmacokinetic Characteristics After Administration of DW4421-T1 and DW4421S-T1 in Healthy Adult Volunteers

Daewon Pharmaceutical Co., Ltd.1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2026年3月6日最近更新:
干预措施

试验速览

阶段
1 期
状态
尚未招募
入组人数
38
试验地点
1
主要终点
Cmax

研究概览

简要总结

Safety and pharmacokinetic characteristics evaluation of DW4421-T1 and DW4421S-T1

研究设计

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

入排标准

年龄范围
19 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adult aged 19 to 50 (inclusive) years
  • Subjects weighing between 50 kg and 90 kg with BMI between 18 and 27 kg/m2 (inclusive)

排除标准

  • clinical significant liver, kidney, nervous system, respiratory, endocrine, hematology and oncology, cardiovascular, urinary, and mental diseases or past history

研究组 & 干预措施

Sequence A

Experimental

cross-over

干预措施: DW4421-T1 (Drug)

Sequence A

Experimental

cross-over

干预措施: DW4421S-T1 (Drug)

Sequence B

Experimental

Cross-over

干预措施: DW4421-T1 (Drug)

Sequence B

Experimental

Cross-over

干预措施: DW4421S-T1 (Drug)

结局指标

主要结局

Cmax

时间窗: up to 48 hour

AUC0-t

时间窗: up to 48 hour

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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