J Drugs Dermatol. 2021 Apr 1;20(4):420-425. doi: 10.36849/JDD.2021.5653.
The fixed dose combination of calcipotriene and betamethasone dipropionate (CAL/BDP) is a well-established, efficacious, and safe topical treatment of psoriasis.
A Phase 3, multicenter, randomized, investigator-blind, active, and vehicle-controlled trial enrolling 796 patients with moderate to severe psoriasis according to the Physician Global Assessment (PGA) scale. Products were applied once daily for 8 weeks.
The proportion of patients achieving PGA treatment success after 8 weeks was statistically significantly greater for CAL/BDP cream (37.4%) compared to CAL/BDP TS (22.8%, P<0.0001), and vehicle (3.7%, P<0.0001). A similar statistically significant difference in favor of CAL/BDP cream at week 8 was demonstrated for the percentage change in mPASI from baseline and the proportion of patients obtaining mPASI75. Patient reported treatment convenience for CAL/BDP cream was rated superior to CAL/BDP TS. Safety assessments during the trial demonstrated that CAL/BDP cream was well-tolerated with no adverse reactions with a frequency greater than 1%.
CAL/BDP cream is a novel topical treatment of psoriasis, which in a single product, offers a unique combination of high efficacy combined with favorable safety and excellent treatment convenience. For these reasons, CAL/BDP cream offers a distinctive advantage for the topical treatment of plaque psoriasis. ClinicalTrials.gov: NCT03308799J Drugs Dermatol. 20(4):420-425. doi:10.36849/JDD.5653.
卡泊三醇倍他米松(CAL/BDP)固定剂量复方制剂是一种成熟的、有效的、安全的治疗银屑病的局部治疗药物。
一项多中心、随机、研究者盲法、阳性药物对照的 3 期临床试验,共纳入 796 例中重度银屑病患者,根据医生总体评估(PGA)量表进行评估。患者每日一次应用研究药物,共 8 周。
8 周后,CAL/BDP 乳膏(37.4%)在治疗成功率方面显著优于 CAL/BDP 洗剂(22.8%,P<0.0001)和赋形剂(3.7%,P<0.0001)。CAL/BDP 乳膏在第 8 周时在从基线的 mPASI 变化百分比和获得 mPASI75 的患者比例方面也具有相似的统计学显著优势。患者对 CAL/BDP 乳膏治疗便利性的评价优于 CAL/BDP 洗剂。试验期间的安全性评估表明,CAL/BDP 乳膏具有良好的耐受性,无不良反应发生率超过 1%。
CAL/BDP 乳膏是一种新型的银屑病局部治疗药物,在单一产品中提供了高疗效与良好的安全性和极佳的治疗便利性相结合的独特组合。由于这些原因,CAL/BDP 乳膏为斑块状银屑病的局部治疗提供了独特的优势。临床试验注册:NCT03308799。J 皮肤病药物学杂志。20(4):420-425。doi:10.36849/JDD.5653.