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     154  0 Kommentare Galapagos announces first dosing in MANGROVE Phase 2 trial with GLPG2737 in polycystic kidney disease - Seite 2

    About Galapagos
    Galapagos (Euronext & NASDAQ: GLPG) discovers and develops small molecule medicines with novel modes of action, several of which show promising patient results and are currently in late-stage development in multiple diseases. The company’s pipeline comprises early discovery through to Phase 3 programs in inflammation, fibrosis, and other indications. Galapagos’ ambition is to become a leading global biopharmaceutical company focused on the discovery, development and commercialization of innovative medicines. More information at www.glpg.com.

    GLPG2737 is an investigational drug and its efficacy and safety have not been established.

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    Den Basisprospekt sowie die Endgültigen Bedingungen und die Basisinformationsblätter erhalten Sie bei Klick auf das Disclaimer Dokument. Beachten Sie auch die weiteren Hinweise zu dieser Werbung.

    For more information about our early clinical programs: www.glpg.com/other-programs
    For information about the studies with GLPG2737 in ADPKD (NCT04578548): www.clinicaltrials.gov

    Contact

    Investors:
    Elizabeth Goodwin
    VP Investor Relations
    +1 781 460 1784

    Sofie Van Gijsel
    Senior Director Investor Relations
    +32 485 19 14 15
    ir@glpg.com

    Media:
    Carmen Vroonen
    Global Head of Communications & Public Affairs
    +32 473 824 874

    Anna Gibbins
    Senior Director Therapeutic Areas Communications
    +44 7717 801900
    communications@glpg.com

    Forward-looking statements

    This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, that are subject to risks, uncertainties and other factors that could cause actual results to differ materially from those referred to in the forward-looking statements and, therefore, the reader should not place undue reliance on them. These risks, uncertainties and other factors include, without limitation, the risk that ongoing and future clinical studies with GLPG2737 may not be completed in the currently envisaged timelines or at all, the inherent uncertainties associated with competitive developments, clinical trial and product development activities and regulatory approval requirements (including that data from the ongoing and planned clinical research programs may not support registration or further development of GLPG2737 due to safety, efficacy or other reasons), Galapagos' reliance on collaborations with third parties, and that Galapagos’ estimations regarding its GLPG2737 development program, regarding the potential value of CFTR inhibition as a mechanism to treat ADPKD, and regarding the commercial potential of GLPG2737, may be incorrect, as well as those risks and uncertainties identified in our Annual Report on Form 20-F for the year ended 31 December 2019 and our subsequent filings with the SEC. All statements other than statements of historical fact are statements that could be deemed forward-looking statements. The forward-looking statements contained herein are based on management’s current expectations and beliefs and speak only as of the date hereof, and Galapagos makes no commitment to update or publicly release any revisions to forward-looking statements in order to reflect new information or subsequent events, circumstances or changes in expectations.

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    Galapagos announces first dosing in MANGROVE Phase 2 trial with GLPG2737 in polycystic kidney disease - Seite 2 Mechelen, Belgium; 1 December 2020, 22.01 CET; Galapagos NV (Euronext & NASDAQ: GLPG) announces first dosing in the new MANGROVE Phase 2 trial with investigational CFTR inhibitor GLPG2737 in patients with autosomal dominant polycystic kidney disease …