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    About us

    Futura Medical is the developer of innovative sexual health products, including lead product Eroxon®. Our core strength lies in our research, development and commercialisation of topically delivered gel formulations in sexual health products. 

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    Eroxon®

    Our lead product is Eroxon®a clinically proven breakthrough treatment for erectile dysfunction

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  • PIPELINE

    PIPELINE

    Futura has two new products in its development pipeline, Eroxon® Intense and WSD4000 for the treatment of sexual dysfunction in men and women.

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    • WSD4000 - For the treatment of sexual dysfunction in women
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    Investor centre

    Futura Medical specialises in the development and global commercialisation of innovative and proprietary sexual health products.  Our lead product is Eroxon®, a clinically proven breakthrough treatment for erectile dysfunctions. 

    We are experts in the research, development and commercialisation of topically delivered gel formulations. 

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        • Futura Medical CEO James Barder on Futura’s 2024 strong growth, maiden profit and 2025 plans
        • Futura Medical announces enhanced Eroxon Gel for ED and female sexual dysfunction product
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        • 2025
          • Panmure Liberum - Futura Medical Learnings will be Key
          • Trinity Delta Futura Medical Home use study supports WSD4000 development
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    • What is Eroxon ® Intense and when will it be available?

      Eroxon® Intense is an additional treatment option for erectile dysfunction that is aimed at helping the cohort of men that may prefer a stronger sensation from Eroxon®.

      We are expecting regulatory approval in the EU and USA by the end of 2025.

    • What is WSD4000 and when will it be available?

      WSD4000 is a topical gel that is being specifically designed to treat symptoms of sexual dysfunction in women, providing improvements in sexual desire, arousal, lubrication, pain during intercourse, orgasm and overall sexual satisfaction. Currently, no regulatory approved topical treatment for sexual dysfunction in women is available over the counter.

      We are unable to provide a firm date for when WSD4000 will become available. A further pre-submission meeting with the FDA has taken place, where good progress was made to clearly define the product’s indication for use, the potential claims, and how these should be proven during the clinical phase of development. Following the FDA meeting and the success of the study we are proceeding  with an Early Feasibility Study to be completed in the first half of 2026. This will enable the Group to consider refinements to the methodology in a population more representative of the target user and therefore hope to increase efficacy still further, as well as further inform on perceptions of the product. WSD4000 has the potential to be an effective breakthrough treatment for the common symptoms of sexual dysfunction in women and is a large and significant commercial opportunity in a market where there are very few treatments available to women .

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