跳至主要内容
临床试验/NCT01346969
NCT01346969已完成2 期

A PHASE 2, RANDOMIZED, DOUBLE-BLIND, WITHIN-SUBJECT CONTROLLED STUDY TO EVALUATE EFFICACY AND SAFETY OF VARIOUS DOSES AND REGIMENS OF EXC 001 FOR THE AMELIORATION OF SCARRING FOLLOWING REVISION OF SCARS FROM PRIOR BREAST SURGERY IN ADULT SUBJECTS (LEGACY EXCALIARD PROTOCOL # EXC 001-204)

Pfizer12 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2011年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Pfizer
入组人数
68
试验地点
12
主要终点
Physician Observer Scar Assessment Score at Week 24

研究概览

简要总结

The study will investigate the efficacy of various doses and regimens of EXC 001 in reducing skin scarring in subjects undergoing revision of scars from prior surgery. The study will also evaluate the safety and tolerability of EXC 001 and placebo.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must have previous had breast surgery resulting in unacceptable scars.
  • Subject has chosen to have breast scars revised.
  • Subject must not be pregnant or lactating.

排除标准

  • Currently pregnant or pregnant during the 6 months, prior to inclusion in the study or lactating.
  • Participation in another clinical trial within 30 days prior to the start of the study.
  • Any other condition or prior therapy, which, in the opinion of the PI, would make the subject unsuitable for the study.

研究组 & 干预措施

Group 1

Active Comparator

干预措施: EXC 001 (Drug)

Group 2

Placebo Comparator

干预措施: EXC 001 (Drug)

Group 3

Placebo Comparator

干预措施: EXC 001 (Drug)

Group 4

Placebo Comparator

干预措施: EXC 001 (Drug)

结局指标

主要结局

Physician Observer Scar Assessment Score at Week 24

时间窗: Week 24

Physician assessment of scar was done using a valid published 10-point rating scale. Physician rated vascularity, pigmentation, thickness, relief, pliability, surface area and overall opinion for scar on a score of 1 = normal skin to 10 = worst scar imaginable, where lower scores indicated better outcome. Composite score was the sum of all the scores, except the overall opinion score, and range from 6 (best score) to 60 (worst score), where lower scores indicated better outcome. Within participant treatment difference was assessed between the treatment regimens each participant received.

次要结局

  • Physician Observer Scar Assessment Score(Week 11, 18)
  • Number of Participants With Physician Photonumeric Guide Scar Assessment Score(Week 24)
  • Subject Observer Scar Assessment Score(Week 24)
  • Number of Participants With Participant Photonumeric Guide Scar Assessment Score(Week 24)
  • Expert Panel Scar Assessment Score(Week 11, 18, 24)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (12)

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