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Improved Ejaculatory Latency, Control and Sexual Satisfaction When PSD502 is Applied Topically in Men with Premature Ejaculation: Results of a Phase III, Double-Blind, Placebo-Controlled Study - ScienceDirect
Absorption Pharmaceuticals and Kaiser Permanente Initiate Clinical Trial of Promescent®
Safety and Pharmacokinetics of PSD502 in Healthy Chinese Male and Female Volunteers: Two Randomized, Double-Blind, Placebo-Controlled, Phase I Trials | SpringerLink
Fortacin USA Availability - PSD502 FDA Approval Process
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PSD502 improves ejaculatory latency, control and sexual satisfaction when applied topically 5 min before intercourse in men with premature ejaculation: results of a phase III, multicentre, double‐blind, placebo‐controlled study - Dinsmore -
PSD502 improves ejaculatory latency, control and sexual satisfaction when applied topically 5 min before intercourse in men with premature ejaculation: results of a phase III, multicentre, double‐blind, placebo‐controlled study - Dinsmore -
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PSD502 improves ejaculatory latency, control and sexual satisfaction when applied topically 5 min before intercourse in men with premature ejaculation: results of a phase III, multicentre, double‐blind, placebo‐controlled study - Dinsmore -
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UPDATE - Plethora Solutions secures manufacturing development partner for PSD502 | AIM:PLE
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Fortacin™ Spray for the Treatment of Premature Ejaculation - Hartmut Porst, Andrea Burri, 2017
Phase 3 Clinical Trials of PSD502 and Dapoxetine in the Treatment of PE | Download Table
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Full article: TEMPE: Topical Eutectic-Like Mixture for Premature Ejaculation
