IMVEXXY offers relief to your patients in as little as 2 weeks1
A healthy sex life starts with a healthy vagina
IMVEXXY reduced moderate to severe dyspareunia due to vulvar and vaginal atrophy at week 12 and as early as week 2 (a secondary endpoint; n=574)1,2
†P<0.0001.
P value vs placebo based on mixed model repeated measures analysis.
This 12-week, randomized, double-blind, placebo-controlled, parallel-group study enrolled 574 generally healthy postmenopausal women aged 40 to 75 years who, at baseline, had ≤5% superficial cells on a vaginal smear, a vaginal pH of >5.0, and self-identified moderate to severe dyspareunia as their most bothersome symptom of vulvar and vaginal atrophy (VVA).2 Participants used the VVA Self-Assessment Questionnaire at screening to identify and assess their most bothersome symptom of VVA, including dyspareunia (scoring: 0 = none, 1 = mild, 2 = moderate, 3 = severe). They were reassessed at weeks 2, 6, 8, and 12.1
Improvement in the mean change from baseline at week 12 was assessed for the coprimary efficacy variables of the most bothersome moderate to severe symptom of dyspareunia, percentage of vaginal superficial and parabasal cells on a vaginal smear, and vaginal pH.2
References: 1. Constantine GD, Simon JA, Pickar JH, et al; REJOICE Study Group. The REJOICE trial: a phase 3 randomized, controlled trial evaluating the safety and efficacy of a novel vaginal estradiol soft-gel capsule for symptomatic vulvar and vaginal atrophy. Menopause. 2017;24(4):409-416. 2. IMVEXXY [package insert]. Raleigh, NC: Mayne Pharma; 2023.