Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Dapoxetine + lidocaine is a combination therapeutic regimen being investigated for the treatment of lifelong premature ejaculation (PE), particularly in patients who are refractory to dapoxetine monotherapy. The regimen consists of oral dapoxetine, a short-acting selective serotonin reuptake inhibitor (SSRI), and a topical 5% lidocaine spray. Dapoxetine acts centrally by inhibiting the serotonin transporter (SERT), thereby increasing serotonin levels and delaying the ejaculatory reflex. Lidocaine acts as a local anesthetic by blocking voltage-gated sodium channels in the sensory nerve fibers of the penis, providing a peripheral desensitizing effect. This dual-action approach aims to provide superior efficacy compared to monotherapy by targeting both central and peripheral pathways involved in ejaculation.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on dapoxetine + lidocaine.