A Phase 2, Multi-Center, Double-Blind, Randomized, Vehicle-Controlled Study to Compare the Safety and Efficacy of IDP-123 Lotion to Tazorac® (Tazarotene) Cream, 0.1%, in the Treatment of Acne Vulgaris
试验速览
- 阶段
- 2 期
- 入组人数
- 210
- 主要终点
- Percent of subjects who achieve at least a two-grade reduction from baseline and are Clear or Almost Clear at Week 12 in the Evaluator's Global Severity Score
研究概览
简要总结
The primary objective of this study is to compare the safety and efficacy of once daily application of IDP-123 Lotion to Tazorac Cream, 0.1%, Vehicle Lotion, and Vehicle Cream in subjects with moderate to severe acne vulgaris.
详细描述
This is a multi-center, randomized, double-blind, vehicle-controlled, 12-week study designed to assess the safety, tolerability, and efficacy of IDP-123 Lotion in comparison with Tazorac Cream, Vehicle Lotion, and Vehicle Cream in subjects with moderate to severe acne. Treatment success will be evaluated by changes in inflammatory and non-inflammatory lesion counts, as well as treatment success using an Evaluator's Global Severity Score. IDP-123 is a lotion for the topical treatment of acne.
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 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female at least 12 years of age and older
- •Written and verbal informed consent must be obtained
- •Subject must have a score of moderate or severe on the Evaluator's Global Severity assessment
- •Pre-menses females and women of childbearing potential must have a negative urine pregnancy test at the screening and baseline visits
- •Subjects must be willing to comply with study instructions and return to the clinic for required visits
排除标准
- •Any dermatological conditions on the face that could interfere with clinical evaluations
- •Any underlying disease(s) or some other dermatological condition of the face that requires the use of interfering topical or systemic therapy or makes evaluations and lesion count inconclusive
- •Subjects with a facial beard or mustache that could interfere with the study assessments
- •Subjects who are unable to communicate or cooperate with the Investigator
- •Subjects with any underlying disease that the Investigator deems uncontrolled, and poses a concern for the subjects safety while participating in the study
研究组 & 干预措施
IDP-123 Lotion
IDP-123 Lotion, applied topically to the face, once daily for 12 weeks.
干预措施: IDP-123 Lotion (Drug)
Tazorac Cream, 0.1%
Tazorac Cream (tazarotene 0.1%), applied topically to the face, once daily for 12 weeks.
干预措施: Tazorac Cream, 0.1%, (Drug)
Vehicle Cream
Vehicle Cream, applied topically to the face, once daily for 12 weeks.
干预措施: Vehicle Cream (Drug)
Vehicle Lotion
Vehicle Lotion, applied topically to the face, once daily for 12 weeks.
干预措施: Vehicle Lotion (Drug)
结局指标
主要结局
Percent of subjects who achieve at least a two-grade reduction from baseline and are Clear or Almost Clear at Week 12 in the Evaluator's Global Severity Score
时间窗: 12 weeks
At each visit the severity will be determined based on evaluator-blinded evaluations of the signs and symptoms of acne vulgaris. Evaluations will be scored on a scale of 0-4 (Evaluator's Global Severity Score), with 0 being clear and 4 being severe. Please see below for complete definitions. 0 - Clear - Normal, clear skin with no evidence of acne vulgaris 1. Almost clear- Rare non-inflammatory lesions present, with rare non-inflamed papules 2. Mild- Some non-inflammatory lesions are present, with few inflammatory lesions (papules/pustules only; no nodulocystic lesions) 3. Moderate-Non-inflammatory lesions predominate, with multiple inflammatory lesions evident: several to many comedones and papules/pustules, and there may or may not be one nodulocystic lesion 4. Severe- Inflammatory lesions are more apparent, many comedones and papules/pustules, there may or may not be up to 2 nodulocystic lesions.
Absolute change in mean inflammatory lesion counts at Week 12
时间窗: 12 weeks
Facial area lesion counts will be taken from the subject's face by the Evaluator at each visit and the change at week 12 from baseline will be calculated. Facial inflammatory lesions (pustules, papules, and nodules) will be counted as follows: pustules and papules will be counted and recorded together, not separately; nodular lesions will be counted and recorded separately. Inflammatory lesions are defined as follows: Papule - a solid, elevated lesion less than 5 mm; Pustule - an elevated lesion containing pus less than 5 mm; Nodule - palpable subcutaneous lesion greater than 5 mm; has depth, not necessarily elevated
Absolute change in mean non-inflammatory lesion counts at Week 12
时间窗: 12 weeks
Facial area lesion counts will be taken from the subject's face by the Evaluator at each visit, and the change at week 12 from baseline will be calculated. Non-inflammatory lesions (open and closed comedones) will be counted and recorded together. Non-inflammatory lesions are defined as follows: Open comedones (blackhead) - plugged hair follicle with dilated/open orifice, black in color; Closed comedones (whitehead) - plugged hair follicle: small opening at skin surface
次要结局
- Mean percent change in inflammatory lesion count from baseline at Weeks 2, 4, 8, and 12.(2, 4, 8, and 12 weeks)
- The proportion of subjects with at least a two grade improvement in the Evaluator's Global Severity Score from baseline at Weeks 2, 4, 8 and 12.(2, 4, 8, and 12 weeks)
- Mean percent change in non-inflammatory lesion counts from baseline at Weeks 2, 4, 8 and 12.(2, 4, 8, and 12 weeks)