A total of 200 participants were randomized to sildenafil cream (n=101) or placebo cream (n=99); 99 sildenafil cream–assigned women and 94 placebo cream–assigned women who received at least one dose of the investigational
A total of 200 participants were randomized to sildenafil cream (n=101) or placebo cream (n=99); 99 sildenafil cream–assigned women and 94 placebo cream–assigned women who received at least one dose of the investigational product made up the ITT population. A total of 174 women (sildenafil 90 and placebo 84) completed all study visits.
Two hundred participants were randomized to either sildenafil cream (n = 101) or placebo cream (n = 99), and 99 sildenafil cream–assigned women and 94 placebo
Published data show that topical Sildenafil Cream, 3.6% was safe and well tolerated by women and their partners across 1,357 sexual experiences. Use of topical Sildenafil Cream, 3.6% did not produce the common side effects of headache and flushing associated with oral sildenafil use in women.
Two hundred participants were randomized to either sildenafil cream (n = 101) or placebo cream (n = 99), and 99 sildenafil cream–assigned women and 94 placebo cream–assigned women received at least 1 dose of their assigned IP in the double-blind dosing period, representing the ITT population.
Therefore, topical Sildenafil Cream, 3.6% (Sildenafil Cream) is being developed for the treatment of FSAD in women. The hypothesis is that by delivering sildenafil topically
Published data show that topical Sildenafil Cream, 3.6% was safe and well tolerated by women and their partners across 1,357 sexual experiences. Use of topical Sildenafil Cream, 3.6% did
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Aims: The study sought to test the systemic and local genital safety of topical sildenafil cream, 3.6% (sildenafil cream) among healthy premenopausal women with FSAD
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