Julie C Harper, L. Stein Gold, Hilary Baldwin, Valerie Callender, Michael Gold, Heather Woolery-Lloyd, L. Kircik
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The objective of this analysis is to assess the impact of age on efficacy, safety, and tolerability in females with moderate-to-severe acne. \nMethods: In one phase 2 (N=741; NCT03170388) and two identically designed phase 3 (N=183; N=180; NCT04214639; NCT04214652), double-blind, randomized, 12-week studies, participants aged ≥9 years with moderate-to-severe acne were randomized to receive once-daily CAB or vehicle gel; the phase 2 study included three additional dyad randomization arms (data not shown). Coprimary endpoints comprised inflammatory and noninflammatory lesion counts and treatment success (≥2-grade reduction from baseline in Evaluator’s Global Severity Score and score of ‘clear’ or ‘almost clear’). Treatment-emergent adverse events (TEAEs) and cutaneous safety and tolerability were also assessed. Pooled data from these studies were analyzed post hoc from female participants categorized by age: 9-24 years (n=274) and ≥25 years (n=121). \nResults: At week 12 in both age groups, least-squares mean percent reductions from baseline were >70% in CAB-treated females versus vehicle gel for inflammatory (9-24 y: 77.8% vs 53.8%; ≥25 y: 77.8% vs 60.5%; P<0.01, both) and noninflammatory lesions (9-24 y: 72.8% vs 44.5%; ≥25 y: 73.7% vs 55.2%; P<0.001, both). Half of CAB-treated females in both age groups achieved treatment success at week 12 versus less than one-quarter with vehicle (9-24 y: 54.1% vs 15.6%; ≥25 y: 50.1% vs 22.5%; P<0.01, both). Most TEAEs were mild-to-moderate in severity, with rates similar to the overall pooled phase 2 and 3 populations. Although there were transient increases in the severity of cutaneous safety/tolerability assessments with CAB, scores generally returned to or near baseline levels for most assessments by week 12 in younger and older females. No notable age-related trends in safety were observed. \nConclusions: With greater than 70% lesion reductions and half of participants achieving treatment success by week 12, the innovative, fixed-dose triple combination clindamycin phosphate 1.2%/adapalene 0.15%/BPO 3.1% gel demonstrated good efficacy, safety, and tolerability in both younger and older females with moderate-to-severe acne. \nFunding: Ortho Dermatologics","PeriodicalId":22013,"journal":{"name":"SKIN The Journal of Cutaneous Medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy and Safety of Clindamycin Phosphate 1.2%/Adapalene 0.15%/Benzoyl Peroxide 3.1% Gel in Females with Moderate to Severe Acne: Post Hoc Analysis by Age\",\"authors\":\"Julie C Harper, L. Stein Gold, Hilary Baldwin, Valerie Callender, Michael Gold, Heather Woolery-Lloyd, L. Kircik\",\"doi\":\"10.25251/skin.8.supp.392\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: While acne is common in adolescents, the overall prevalence in adults is increasing, especially among females. In addition, acne in older females is associated with greater negative impacts on quality of life. Clindamycin phosphate 1.2%/adapalene 0.15%/benzoyl peroxide (BPO) 3.1% (CAB) gel—the first fixed-dose, triple-combination topical product approved for acne—has demonstrated good efficacy, safety, and tolerability in participants with moderate-to-severe acne. The objective of this analysis is to assess the impact of age on efficacy, safety, and tolerability in females with moderate-to-severe acne. \\nMethods: In one phase 2 (N=741; NCT03170388) and two identically designed phase 3 (N=183; N=180; NCT04214639; NCT04214652), double-blind, randomized, 12-week studies, participants aged ≥9 years with moderate-to-severe acne were randomized to receive once-daily CAB or vehicle gel; the phase 2 study included three additional dyad randomization arms (data not shown). Coprimary endpoints comprised inflammatory and noninflammatory lesion counts and treatment success (≥2-grade reduction from baseline in Evaluator’s Global Severity Score and score of ‘clear’ or ‘almost clear’). Treatment-emergent adverse events (TEAEs) and cutaneous safety and tolerability were also assessed. Pooled data from these studies were analyzed post hoc from female participants categorized by age: 9-24 years (n=274) and ≥25 years (n=121). \\nResults: At week 12 in both age groups, least-squares mean percent reductions from baseline were >70% in CAB-treated females versus vehicle gel for inflammatory (9-24 y: 77.8% vs 53.8%; ≥25 y: 77.8% vs 60.5%; P<0.01, both) and noninflammatory lesions (9-24 y: 72.8% vs 44.5%; ≥25 y: 73.7% vs 55.2%; P<0.001, both). Half of CAB-treated females in both age groups achieved treatment success at week 12 versus less than one-quarter with vehicle (9-24 y: 54.1% vs 15.6%; ≥25 y: 50.1% vs 22.5%; P<0.01, both). Most TEAEs were mild-to-moderate in severity, with rates similar to the overall pooled phase 2 and 3 populations. Although there were transient increases in the severity of cutaneous safety/tolerability assessments with CAB, scores generally returned to or near baseline levels for most assessments by week 12 in younger and older females. 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引用次数: 0
摘要
导言:痤疮在青少年中很常见,但在成年人中的总体发病率却在不断上升,尤其是女性。此外,老年女性的痤疮对生活质量的负面影响更大。克林霉素磷酸酯 1.2%/阿达帕林 0.15%/过氧化苯甲酰(BPO)3.1%(CAB)凝胶是首个获准用于治疗痤疮的固定剂量三合一外用产品,在中重度痤疮患者中显示出良好的疗效、安全性和耐受性。本分析旨在评估年龄对中重度痤疮女性患者的疗效、安全性和耐受性的影响。研究方法在一项2期研究(N=741;NCT03170388)和两项设计相同的3期研究(N=183;N=180;NCT04214639;NCT04214652)、双盲、随机、为期12周的研究中,年龄≥9岁的中度至重度痤疮患者被随机分配接受每日一次的CAB或载体凝胶;2期研究包括三个额外的双组随机分组(数据未显示)。主要终点包括炎症性和非炎症性皮损计数和治疗成功率(评价者总体严重程度评分和 "痊愈 "或 "基本痊愈 "评分比基线降低≥2级)。此外,还评估了治疗突发不良事件(TEAE)以及皮肤安全性和耐受性。对这些研究的汇总数据进行了事后分析,女性参与者按年龄分为:9-24 岁(274 人)和≥25 岁(121 人)。研究结果第 12 周时,在两个年龄组中,经 CAB 治疗的女性炎症性病变(9-24 岁:77.8% vs 53.8%;≥25 岁:77.8% vs 60.5%;P<0.01,均相同)和非炎症性病变(9-24 岁:72.8% vs 44.5%;≥25 岁:73.7% vs 55.2%;P<0.001,均相同)与药物凝胶相比,最小二乘平均百分比从基线降低了 70% 以上。在两个年龄组中,一半接受过CAB治疗的女性在第12周时取得了治疗成功,而接受药物治疗的女性只有不到四分之一取得了治疗成功(9-24岁:54.1% vs 15.6%;≥25岁:50.1% vs 22.5%;P<0.01,两者均如此)。大多数TEAE的严重程度为轻度至中度,其发生率与第2和第3阶段的总体汇总人群相似。虽然皮肤安全性/耐受性评估的严重程度会随着 CAB 的使用而短暂增加,但在第 12 周之前,年轻女性和老年女性的大多数评估得分普遍恢复到或接近基线水平。在安全性方面没有观察到明显的年龄相关趋势。结论克林霉素磷酸酯1.2%/阿达帕林0.15%/BPO 3.1%凝胶是一种创新的固定剂量三联疗法,在中度至重度痤疮的年轻女性和老年女性中,其皮损减少率超过70%,半数参与者在第12周时取得了治疗成功,显示出良好的疗效、安全性和耐受性。资金来源:Ortho DermatologicsOrtho Dermatologics
Efficacy and Safety of Clindamycin Phosphate 1.2%/Adapalene 0.15%/Benzoyl Peroxide 3.1% Gel in Females with Moderate to Severe Acne: Post Hoc Analysis by Age
Introduction: While acne is common in adolescents, the overall prevalence in adults is increasing, especially among females. In addition, acne in older females is associated with greater negative impacts on quality of life. Clindamycin phosphate 1.2%/adapalene 0.15%/benzoyl peroxide (BPO) 3.1% (CAB) gel—the first fixed-dose, triple-combination topical product approved for acne—has demonstrated good efficacy, safety, and tolerability in participants with moderate-to-severe acne. The objective of this analysis is to assess the impact of age on efficacy, safety, and tolerability in females with moderate-to-severe acne.
Methods: In one phase 2 (N=741; NCT03170388) and two identically designed phase 3 (N=183; N=180; NCT04214639; NCT04214652), double-blind, randomized, 12-week studies, participants aged ≥9 years with moderate-to-severe acne were randomized to receive once-daily CAB or vehicle gel; the phase 2 study included three additional dyad randomization arms (data not shown). Coprimary endpoints comprised inflammatory and noninflammatory lesion counts and treatment success (≥2-grade reduction from baseline in Evaluator’s Global Severity Score and score of ‘clear’ or ‘almost clear’). Treatment-emergent adverse events (TEAEs) and cutaneous safety and tolerability were also assessed. Pooled data from these studies were analyzed post hoc from female participants categorized by age: 9-24 years (n=274) and ≥25 years (n=121).
Results: At week 12 in both age groups, least-squares mean percent reductions from baseline were >70% in CAB-treated females versus vehicle gel for inflammatory (9-24 y: 77.8% vs 53.8%; ≥25 y: 77.8% vs 60.5%; P<0.01, both) and noninflammatory lesions (9-24 y: 72.8% vs 44.5%; ≥25 y: 73.7% vs 55.2%; P<0.001, both). Half of CAB-treated females in both age groups achieved treatment success at week 12 versus less than one-quarter with vehicle (9-24 y: 54.1% vs 15.6%; ≥25 y: 50.1% vs 22.5%; P<0.01, both). Most TEAEs were mild-to-moderate in severity, with rates similar to the overall pooled phase 2 and 3 populations. Although there were transient increases in the severity of cutaneous safety/tolerability assessments with CAB, scores generally returned to or near baseline levels for most assessments by week 12 in younger and older females. No notable age-related trends in safety were observed.
Conclusions: With greater than 70% lesion reductions and half of participants achieving treatment success by week 12, the innovative, fixed-dose triple combination clindamycin phosphate 1.2%/adapalene 0.15%/BPO 3.1% gel demonstrated good efficacy, safety, and tolerability in both younger and older females with moderate-to-severe acne.
Funding: Ortho Dermatologics