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临床试验/NCT04782505
NCT04782505已完成1 期

A Open-label, Single-dose, Phase 1 Study to Compare and Evaluate the Safety and Pharmacokinetics According to the Dose of Camostat Mesylate in Healthy Volunteers

Daewoong Pharmaceutical Co. LTD.1 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2021年3月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
61
试验地点
1
主要终点
Cmax of GBPA

研究概览

简要总结

Safety and pharmacokinetics evaluation study according to the dose of camostat mesylate in healthy volunteers

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 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged ≥ 19 and ≤ 55 years at screening
  • Subjects with body weight of ≥ 55.0 kg and ≤ 90.0 kg, and a body mass index (BMI) of ≥ 18.0 and ≤ 29.9
  • Subjects who have no congenital or chronic disease and have no pathological symptoms or findings as a result of an internal examination

排除标准

  • Subjects with current or prior history of a clinically significant hepatic, renal, nervous, respiratory, gastrointestinal, endocrine, hematologic and oncologic, urogenital, cardiovascular, musculoskeletal or psychiatric disorder
  • Subjects with symptoms of acute disease within 28 days prior to the scheduled first administration date of IP
  • Subjects with a history of gastrointestinal diseases (e.g., Crohn's disease, ulcers, etc.) or gastrointestinal resection (except simple appendectomy or hernia surgery) that may affect the absorption of drugs.

研究组 & 干预措施

Cohort 1 (Part 1)

Experimental

DWJ1248 100mg (100mg 1tab) PO

干预措施: DWJ1248 (Drug)

Cohort 2 (Part 1)

Experimental

DWJ1248 200mg (100mg 2tab) PO

干预措施: DWJ1248 (Drug)

Cohort 3 (Part 1)

Experimental

DWJ1248 300mg (100mg 3tab) PO

干预措施: DWJ1248 (Drug)

Group A (Part 2)

Experimental

DWJ1248 100mg 2tab PO - Wash out - DWJ1248 200mg 1tab PO

干预措施: DWJ1248 (Drug)

Group B (Part 2)

Experimental

DWJ1248 200mg 1tab PO - Wash out - DWJ1248 100mg 2tab PO

干预措施: DWJ1248 (Drug)

结局指标

主要结局

Cmax of GBPA

时间窗: 0-6 hr

Maximum blood concentration of GBPA (GUANIDINO BENZOYLOXY PHENYLACETIC ACID METHANESULFONATE) among observed blood concentrations at time points * Immediately before administration of IP * After administration

AUClast of GBPA

时间窗: 0-6 hr

Area under the blood concentration-time of GBPA (GUANIDINO BENZOYLOXY PHENYLACETIC ACID METHANESULFONATE) among observed blood concentrations at time points * Immediately before administration of IP * After administration

次要结局

未报告次要终点

研究者

发起方
Daewoong Pharmaceutical Co. LTD.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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