跳至主要内容
临床试验/NCT03184363
NCT03184363Unknown3 期

Efficacy and Safety of DWP450 for Treating Crows Feet Lines(CFL) in Combination With Glabellar Lines: Multi-center, Single Arm, Open, Extension Study

Daewoong Pharmaceutical Co. LTD.0 个研究点目标入组 102 人开始时间: 2017年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
102
主要终点
Subject Assessment of Satisfaction of Appearance

研究概览

简要总结

The purpose of this study is to explore the Efficacy and Safety of DWP450 for treating Crows Feet Lines(CFL) in combination with glabellar line(GL) as extension study of phase 3 study for CFL.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female of at least 18 to 75 years old
  • moderate-to-severe CFL at maximum smile on the FWS as rated by the investigator
  • moderate-to-severe GL at maximum frawn on the FWS as rated by the investigator
  • Subject who has completed phase 3 study for CFL.

排除标准

  • 未提供

研究组 & 干预措施

Clostridium Botulinum A Toxin

Experimental

Clostridium Botulinum A Toxin

干预措施: Clostridium Botulinum A Toxin (Drug)

结局指标

主要结局

Subject Assessment of Satisfaction of Appearance

时间窗: At 4 weeks

Subject Assessment of Satisfaction of Appearance

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

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