Department of Dermatology, University Hospital Frankfurt am Main, Frankfurt am Main, Germany.
Department of Dermatology, University of Rzeszow, Rzeszów, Poland.
J Eur Acad Dermatol Venereol. 2023 Nov;37(11):2327-2335. doi: 10.1111/jdv.19330. Epub 2023 Aug 25.
The fixed dose combination of calcipotriene (CAL) and betamethasone dipropionate (BDP) is a well-established topical treatment option for psoriasis based on strong scientific rationale for the single agents having complementary efficacy and safety. CAL/BDP PAD-cream is an easily spreadable cream based on PAD Technology™, an innovative formulation and drug delivery system.
A Phase 3, multicentre, randomized, investigator-blind, active and vehicle-controlled trial enrolling 490 patients with mild to moderate psoriasis according to the Physician Global Assessment (PGA) scale was conducted in three European countries. Products were applied once daily for 8 weeks. The aim of the trial was to evaluate the efficacy and safety of CAL/BDP PAD-cream as well as treatment acceptability compared to CAL/BDP gel and PAD-cream vehicle. Primary endpoint was percentage change in modified Psoriasis Area and Severity Index (mPASI) from baseline to Week 8.
The percentage mean change from baseline to Week 8 in mPASI for CAL/BDP PAD-cream (67.5%) was superior compared to PAD-cream vehicle (11.7%; p < 0.0001) and non-inferior to CAL/BDP gel (63.5%). The proportion of patients achieving PGA treatment success (at least two-step improvement to clear or almost clear) after 8 weeks was superior for CAL/BDP PAD-cream (50.7%) compared to PAD-cream vehicle (6.1%, p < 0.0001) and statistically significantly greater than CAL/BDP gel (42.7%, p = 0.0442). Patient-reported psoriasis treatment convenience score (PTCS) for CAL/BDP PAD-cream was rated superior to CAL/BDP gel at Week 8 (p < 0.0001) and the mean change in DLQI from baseline to Week 8 improved statistically significantly more in the CAL/BDP PAD-cream group compared to both PAD-cream vehicle (p < 0.0001) and CAL/BDP gel (p = 0.0110). Safety assessments during the trial demonstrated that CAL/BDP PAD-cream was well-tolerated.
CAL/BDP PAD-cream is a novel topical treatment of psoriasis that has a high efficacy and a favourable safety profile combined with a superior patient-reported treatment convenience.
卡泊三醇(CAL)和倍他米松二丙酸酯(BDP)的固定剂量组合是一种成熟的局部治疗选择,适用于银屑病,其基于单一药物具有互补疗效和安全性的强有力科学依据。CAL/BDP PAD-乳膏是一种基于 PAD 技术的易于涂抹的乳膏,这是一种创新的配方和药物传递系统。
在三个欧洲国家进行了一项为期 8 周、多中心、随机、研究者盲法、阳性药物对照的 III 期临床试验,共纳入 490 名轻度至中度银屑病患者(根据医师总体评估 [PGA] 量表)。产品每天应用一次,共 8 周。该试验的目的是评估 CAL/BDP PAD-乳膏的疗效和安全性,并与 CAL/BDP 凝胶和 PAD-乳膏载体相比评估其治疗可接受性。主要终点是从基线到第 8 周时改良银屑病面积和严重程度指数(mPASI)的百分比变化。
CAL/BDP PAD-乳膏(67.5%)的平均基线至第 8 周 mPASI 百分比变化明显优于 PAD-乳膏载体(11.7%;p<0.0001),与 CAL/BDP 凝胶(63.5%)相比非劣效。8 周后,PGA 治疗成功(至少改善两个等级,达到清除或几乎清除)的患者比例,CAL/BDP PAD-乳膏(50.7%)明显高于 PAD-乳膏载体(6.1%,p<0.0001),且明显高于 CAL/BDP 凝胶(42.7%,p=0.0442)。CAL/BDP PAD-乳膏治疗便利性评分(PTCS)在第 8 周时明显优于 CAL/BDP 凝胶(p<0.0001),且从基线到第 8 周时 DLQI 平均变化明显优于 PAD-乳膏载体(p<0.0001)和 CAL/BDP 凝胶(p=0.0110)。试验期间的安全性评估表明,CAL/BDP PAD-乳膏具有良好的耐受性。
CAL/BDP PAD-乳膏是一种治疗银屑病的新型局部治疗方法,疗效高,安全性好,且患者报告的治疗便利性也较好。