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    With Fermion, start the journey of your innovative API.

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    Suanfarma, at the Core of a Better Life.

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    Bionxt Advances Sublingual Drug Delivery With Global Patents
    Bionxt Advances Sublingual Drug Delivery With Global Patents

    24 Mar 2026

    // PHARMIWEB

    https://www.pharmiweb.com/press-release/2026-03-24/bionxt-enters-commercialization-phase-with-global-patent-protection-and-us-fast-track-strategy-for

    PHARMIWEB
    24 Mar 2026
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    BioNxt Advances MS ODF Program Toward Human Trials
    BioNxt Advances MS ODF Program Toward Human Trials

    26 Jan 2026

    // PHARMIWEB

    https://www.pharmiweb.com/press-release/2026-01-26/bionxt-accelerates-odf-for-multiple-sclerosis-toward-human-clinical-study-with-40-bioavailability

    PHARMIWEB
    26 Jan 2026
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    BioNxt Announces Success in Final Cladribine ODF In Vivo Study
    BioNxt Announces Success in Final Cladribine ODF In Vivo Study

    19 Jan 2026

    // PHARMIWEB

    https://www.pharmiweb.com/press-release/2026-01-19/bionxt-reports-successful-final-in-vivo-dosing-study-results-supporting-superior-bioavailability-of

    PHARMIWEB
    19 Jan 2026
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    BioNxt Enhances Cladribine Formulation For MS Patients
    BioNxt Enhances Cladribine Formulation For MS Patients

    09 Dec 2025

    // ACCESSWIRE

    https://www.accessnewswire.com/newsroom/en/healthcare-and-pharmaceutical/bionxt-advances-%22melt-in-your-mouth%22-cladribine-formulation-to-improv-1115793

    ACCESSWIRE
    09 Dec 2025
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    Hopewell’s Generics Cladribine Receives Tentative Approval in US
    Hopewell’s Generics Cladribine Receives Tentative Approval in US

    04 Dec 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215547

    FDA
    04 Dec 2025
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    Apotex’s Receives First Generic Approval for Cladribine in US
    Apotex’s Receives First Generic Approval for Cladribine in US

    24 Nov 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&varApplNo=218425

    FDA
    24 Nov 2025
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