Johnson Isabella, Thurman Andrea Ries, Cornell Katherine A, Dart Clint, Hatheway Jessica, Friend David R, Goldstein Andrew
Daré Bioscience, San Diego, CA, United States.
Strategic Science & Technologies, LLC, Cambridge, MA, United States.
Sex Med. 2024 Nov 19;12(5):qfae079. doi: 10.1093/sexmed/qfae079. eCollection 2024 Oct.
A study of topical Sildenafil Cream 3.6% was completed among healthy premenopausal women with female sexual arousal disorder.
To compare efficacy endpoints based on product use in pre-planned and post-hoc subsets of age, race, and medication use.
Phase 2b, exploratory, randomized, placebo-controlled, double-blind study of Sildenafil Cream, 3.6% among healthy premenopausal women with female sexual arousal disorder (FSAD). Eligible participants were randomized 1:1 to Sildenafil versus Placebo Cream and used investigational product for 12 weeks.
The co-primary efficacy endpoints were the change from baseline, at week 12, in the Arousal Sensation (AS) domain of the Sexual Function Questionnaire (SFQ28) and Question 14 (Q14) of the Female Sexual Distress Scale - Desire, Arousal, Orgasm (FSDS-DAO). The secondary efficacy endpoint was the change from baseline at week 12 in the mean number of satisfactory sexual events (SSEs) reported in a daily diary. Exploratory efficacy endpoints included the Desire and Orgasm domains of the SFQ28.
Age group (≥18 years and ≤ 45 years versus >45 years), race group (White versus non-White), and baseline use/non-use of hormonal contraception did not significantly affect the co-primary endpoints of the SFQ28 AS domain and FSDS-DAO Q14 ( values >0.11). Non-White Sildenafil Cream users had an increase in SSEs at week 12 (0.7 ± 0.63) while non-white Placebo Cream users reported a decrease (-1.5 ± 0.58) ( = .02). Daily psychiatric medication use among women assigned to either Placebo or Sildenafil Cream resulted in lower SFQ28 Desire domain scores compared to non-users of these medications. Women who used study product only in un-partnered events had a larger improvement in their SFQ28 Orgasm domain scores at week 12 (2.39 ± 0.95) with Sildenafil Cream use compared to Placebo (-0.19 ± 0.75) ( = .06). Non-White women represented a higher proportion of un-partnered women and women who used IP only during un-partnered sexual events compared to White women ( < .01).
These pre-planned subset analyses will help refine target populations in future studies of Sildenafil Cream, 3.6% for the treatment of FSAD.
Subset analyses focused on variables pertinent to future target populations. The current study population was primarily educated non-Hispanic White women.
Age and hormonal contraceptive use did not impact the efficacy of topical Sildenafil Cream. Daily psychiatric medication use decreased sexual desire in active and placebo users.
一项针对患有女性性唤起障碍的健康绝经前女性的3.6%西地那非乳膏研究已完成。
基于年龄、种族和药物使用的预先计划和事后亚组中的产品使用情况比较疗效终点。
对患有女性性唤起障碍(FSAD)的健康绝经前女性进行2b期探索性随机安慰剂对照双盲研究,使用3.6%西地那非乳膏。符合条件的参与者按1:1随机分为西地那非组和安慰剂乳膏组,并使用研究产品12周。
共同主要疗效终点是性功能问卷(SFQ28)的唤起感觉(AS)领域和女性性困扰量表-欲望、唤起、性高潮(FSDS-DAO)的问题14(Q14)在第12周时相对于基线的变化。次要疗效终点是每日日记中报告的满意性事件(SSE)平均数在第12周时相对于基线的变化。探索性疗效终点包括SFQ28的欲望和性高潮领域。
年龄组(≥18岁且≤45岁与>45岁)、种族组(白人与非白人)以及基线时使用/未使用激素避孕措施对SFQ28 AS领域和FSDS-DAO Q14的共同主要终点没有显著影响(P值>0.11)。非白人西地那非乳膏使用者在第12周时SSE增加(0.7±0.63),而非白人安慰剂乳膏使用者报告减少(-1.5±0.58)(P = 0.02)。与未使用这些药物的女性相比,分配到安慰剂或西地那非乳膏组的女性每日使用精神科药物导致SFQ28欲望领域得分较低。仅在无伴侣性行为中使用研究产品的女性在第12周时使用西地那非乳膏与安慰剂相比,其SFQ28性高潮领域得分改善更大(2.39±0.95)与(-0.19±0.75)(P = 0.06)。与白人女性相比,非白人女性中无伴侣女性以及仅在无伴侣性行为中使用研究产品的女性所占比例更高(P < 0.01)。
这些预先计划的亚组分析将有助于在未来研究3.6%西地那非乳膏治疗FSAD时优化目标人群。
亚组分析关注与未来目标人群相关的变量。当前研究人群主要是受过教育的非西班牙裔白人女性。
年龄和激素避孕措施的使用不影响外用西地那非乳膏的疗效。每日使用精神科药物会降低活性药物和安慰剂使用者的性欲。