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临床试验/NCT01241331
NCT01241331已完成2 期

A Randomized, Controlled Evaluation of the Safety and Efficacy of a Topical Treatment for Moderate-Severe Facial Acne Vulgaris

Braintree Laboratories20 个研究点 分布在 1 个国家目标入组 233 人开始时间: 2010年11月最近更新:
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
入组人数
233
试验地点
20
主要终点
percent reduction of total acne lesion counts

研究概览

简要总结

The purpose of this study is to compare the safety and efficacy of formulation BLI1100 to its vehicle in the treatment of moderate-severe acne vulgaris.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
12 Years 至 45 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Qualifying Investigator's Global Assessment severity score
  • Qualifying number of non-inflammatory lesions
  • Qualifying number of inflammatory lesions

排除标准

  • Facial hair (beard), excessive scarring, sunburn or other disfigurement that may obscure the accurate assessment of acne grade
  • Using medications that are reported to exacerbate acne
  • Any clinically relevant finding at their baseline physical examination or dermatological medical history such as severe systemic diseases or diseases of the facial skin
  • Have a known hypersensitivity or previous allergic reaction to any of the components
  • Patients who have participated in an investigational clinical, surgical, drug, or device study within the past 30 days
  • Patients who, in the opinion of the investigator, should not be included in the study for any reason, including inability to follow study procedures

研究组 & 干预措施

BLI1100

Experimental

BLI1100 topical cream

干预措施: BLI1100 (Drug)

Vehicle cream

Placebo Comparator

Vehicle topical cream

干预措施: Vehicle cream (Drug)

结局指标

主要结局

percent reduction of total acne lesion counts

时间窗: 12 weeks

次要结局

  • Investigator's Global Assessment(12)
  • Change in serum chemistry(12 weeks)

研究者

发起方
Braintree Laboratories
申办方类型
Industry
责任方
Sponsor

研究点 (20)

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