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临床试验/NCT02108288
NCT02108288已完成1 期

Pharmacokinetic Study of OPC-1085EL Ophthalmic Solution in Healthy Male Adult Volunteers

Otsuka Pharmaceutical Co., Ltd.0 个研究点目标入组 30 人开始时间: 2014年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
30
主要终点
Cmax of Carteolol

研究概览

简要总结

OPC-1085EL ophthalmic solution, carteolol long-acting ophthalmic solution or latanoprost ophthalmic solution are administered once daily for 7 days and the effect on the blood concentration of carteolol and latanoprost in OPC-1085EL ophthalmic solution by formulating the combination drug will be determined.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

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

入选标准

  • Subjects who are considered medically healthy per investigator's judgment

排除标准

  • Subjects with ocular conditions as defined by the protocol
  • Subjects with intraocular pressure: <10 or ≥22 mmHg

研究组 & 干预措施

OPC-1085EL ophthalmic solution

Experimental

Once daily

干预措施: OPC-1085EL ophthalmic solution (Drug)

Carteolol long-acting ophthalmic solution

Active Comparator

Once daily

干预措施: Carteolol long-acting ophthalmic solution (Drug)

Latanoprost ophthalmic solution

Active Comparator

Once daily

干预措施: Latanoprost ophthalmic solution (Drug)

结局指标

主要结局

Cmax of Carteolol

时间窗: Day 1 and Day 7

Cmax of Latanoprost Acid

时间窗: Day 1 and Day 7

次要结局

  • Tmax of Carteolol(Day 1 and Day 7)
  • Tmax of Latanoprost Acid(Day 1 and Day 7)

研究者

申办方类型
Industry
责任方
Sponsor

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