跳至主要内容
临床试验/NCT01780077
NCT01780077已完成1 期

A Phase 1 Single Center, Randomized, Double-Blind, Ascending, Multi-Dose, Within-Subject Controlled Study of RXI-109 for the Treatment of Incision Scars Made in the Abdominal Skin of Healthy Subjects

RXi Pharmaceuticals, Corp.0 个研究点目标入组 15 人开始时间: 2012年12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
发起方
入组人数
15
主要终点
To assess the safety and tolerability of multiple intradermal administrations of RXI-109

研究概览

简要总结

The purpose of this trial is to evaluate the safety and tolerability of multiple (3) intradermal doses of RXI-109 at small surgical incisions in the abdominal skin of healthy volunteers. The effect of RXI-109 versus placebo on scarring at these incision sites will be evaluated visually, histologically, and by biomarker analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Males and females, 21-50 years of age
  • General good health; if female not pregnant or lactating
  • Phototype 3 and above based on the Fitzpatrick scale.

排除标准

  • Pregnant or lactating
  • Use of tobacco or nicotine-containing products within 1 month prior to enrollment and while on study
  • Type 1 or 2 diabetes mellitus
  • A history or presence of any medical condition or therapy that would make the subject an unsafe candidate in the opinion of the investigator

研究组 & 干预措施

RXI-109

Experimental

干预措施: RXI-109 (Drug)

RXI-109

Experimental

干预措施: Placebo (Drug)

Placebo

Placebo Comparator

干预措施: RXI-109 (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

To assess the safety and tolerability of multiple intradermal administrations of RXI-109

时间窗: 12 weeks

Evaluate safety and tolerability of multiple administrations of RXI-109 at the site of intradermal injection. Examine and assess any and all local and systemic toxicities

次要结局

  • To assess the effect of multiple intradermal administrations of RXI-109 on scar formation(12 weeks)

研究者

发起方
RXi Pharmaceuticals, Corp.
申办方类型
Industry
责任方
Sponsor

相似试验