CTRI/2023/10/058218已完成Unknown
A clinical study to evaluate Safety, In-Use Tolerability and Efficacy of HARF-042202 in healthy adults with mild to moderate acne and acne prone skin. - NI
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 102
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1)Subjects having good general health as determined by the Investigator on the basis of medical history. Subjects with acne-prone skin and with mild to moderate acne condition as per IGA scale and acne prone skin.
- •2)Subjects with oily skin having Sebumeter measurement > 180 (µg/cm2).
- •3)Female subjects of childbearing potential must have a negative urine pregnancy test performed on screening and enrolment visit.
- •4)Subjects who are not under any dermatologic treatment for acne and scar/ prescribed medications.
排除标准
- •1)Subjects with drug induced acne as disclosed by subjects.
- •2)Subjects undergoing treatment for skin lightening or subjects using other marketed skin lightening products during the study period or in the past 6 weeks.
- •3)Subjects who are receiving topical or systemic treatments for acne or acne marks.
- •4)Subjects receiving medications (e.g., steroids or anti-histamines) which would compromise the study.
研究者
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