(Lidocaine + prilocaine) is under clinical development by Plethora Solutions and currently in Phase II for Premature Ejaculation. According to GlobalData, Phase II drugs for Premature Ejaculation does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the (Lidocaine + prilocaine) LoA Report. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

(Lidocaine + prilocaine) overview

Lidocaine and Prilocaine (Fortacin / Senstend) is a fixed dose combination. It is formulated as a spray for cutaneous and topical route of administration. It is indicated for the treatment of primary premature ejaculation in adult men and is used to treat men with primary (lifelong) premature ejaculation (when ejaculation regularly occurs before, or too early during penetration). It is under development for the treatment of premature ejaculation in adult man in the US.

Plethora Solutions overview

Plethora Solutions (Plethora), a subsidiary of Regent Pacific is a pharmaceutical company which develops and markets products for the treatment and management of urological disorders.

For a complete picture of (Lidocaine + prilocaine)’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.