Stein Gold Linda, Jackson J Mark, Knuckles Melissa L F, Weiss Jonathan S
J Drugs Dermatol. 2016 Mar;15(3):334-42.
A novel formulation of 0.05% betamethasone dipropionate in an emollient spray vehicle (DFD-01) was developed to deliver steroid to the skin layers most affected by psoriasis.
To compare the efficacy and safety of DFD-01 to its vehicle for the treatment of moderate plaque psoriasis over 4 weeks.
Two Phase 3 trials enrolled adults with moderate psoriasis (Investigator Global Assessment [IGA]=3; 10-20% body surface area [BSA]) and randomized them 2:1 to DFD-01 or Vehicle. Products were applied twice daily to affected areas for 28 days. Treatment success was defined as an IGA=0 or 1 and ≥ 2-grade improvement from baseline. Primary endpoint was the proportion of subjects achieving treatment success at day 15.
Moderate psoriasis subjects were enrolled in Study 1 (174 DFD-01; 87 Vehicle) and Study 2 (182 DFD-01; 95 Vehicle). Mean BSA was 13-14%. Treatment success was achieved in significantly more subjects using DFD-01 than Vehicle at day 15 in both Study 1 (P<0.001) and Study 2 (P=0.002), and at day 29 (both studies P<0.001). Treatment success with DFD-01 was significant at day 8 in Study 1 (P=0.003) but not in Study 2 (P=0.156). Erythema, scaling, and plaque elevation scores of target lesions were significantly reduced as early as day 4 with DFD-01. Adverse events were similar between groups, with no increase between 2 and 4 weeks.
These studies demonstrate DFD-01's excellent efficacy and safety for the treatment of extensive psoriasis (10-20% BSA). DFD-01 achieved treatment success in significantly more subjects than Vehicle after 2 and 4 weeks of treatment, and showed early onset of action with improved signs of erythema, scaling and elevation of target lesions after 4 days of treatment. This medium potency formulation provides a safe and effective choice for topical steroid treatment of psoriasis.
研发了一种新型制剂,即0.05%丙酸倍他米松的润肤喷雾剂型(DFD - 01),用于将类固醇输送到受银屑病影响最严重的皮肤层。
比较DFD - 01及其赋形剂治疗中度斑块状银屑病4周的疗效和安全性。
两项3期试验纳入了中度银屑病成人患者(研究者整体评估[IGA]=3;体表面积[BSA]为10 - 20%),并将他们以2:1的比例随机分为DFD - 01组或赋形剂组。产品每天两次涂抹于患处,持续28天。治疗成功定义为IGA = 0或1且较基线改善≥2级。主要终点是在第15天达到治疗成功的受试者比例。
中度银屑病受试者被纳入研究1(174例DFD - 01;87例赋形剂)和研究2(182例DFD - 01;95例赋形剂)。平均BSA为13 - 14%。在研究1(P<0.001)和研究2(P = 0.002)中,第15天使用DFD - 01的受试者实现治疗成功的人数显著多于赋形剂组,在第29天也是如此(两项研究P<0.001)。在研究1中,DFD - 01在第8天的治疗成功具有显著性(P = 0.003),但在研究2中不显著(P = 0.156)。使用DFD - 01,早在第4天靶皮损的红斑、鳞屑和斑块隆起评分就显著降低。两组间不良事件相似,在2至4周内无增加。
这些研究证明DFD - 01治疗广泛银屑病(10 - 20% BSA)具有出色的疗效和安全性。治疗2周和4周后,使用DFD - 01实现治疗成功的受试者显著多于赋形剂组,且治疗4天后显示出早期起效,靶皮损的红斑、鳞屑和隆起体征得到改善。这种中效制剂为银屑病的局部类固醇治疗提供了一种安全有效的选择。