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Document 62019TN0792

    Case T-792/19: Action brought on 11 November 2019 — Agepha Pharma v EUIPO — Apogepha Arzneimittel (AGEPHA)

    OJ C 10, 13.1.2020, p. 50–51 (BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

    Date of document:
    11/11/2019
    Date lodged:
    11/11/2019
    Author:
    General Court
    Form:
    Judicial information
    Authentic language:
    German
    Type of procedure:
    Action for annulment
    Defendant:
    European Union Intellectual Property Office
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    Select all documents mentioning this document
    Instruments cited in case law:
    Link

    13.1.2020   

    EN

    Official Journal of the European Union

    C 10/50

    Action brought on 11 November 2019 — Agepha Pharma v EUIPO — Apogepha Arzneimittel (AGEPHA)

    (Case T-792/19)

    (2020/C 10/61)

    Language in which the application was lodged: German

    Parties

    Applicant: Agepha Pharma s. r. o. (Senec, Slovakia) (represented by: D. Göbel, lawyer)

    Defendant: European Union Intellectual Property Office (EUIPO)

    Other party to the proceedings before the Board of Appeal: Apogepha Arzneimittel GmbH (Dresden, Germany)

    Details of the proceedings before EUIPO

    Applicant for the trade mark at issue: Applicant

    Trade mark at issue: Application for EU word mark AGEPHA — EU trade mark application No 7 007 909

    Procedure before EUIPO: Opposition proceedings

    Contested decision: Decision of the Second Board of Appeal of EUIPO of 26 August 2019 in Case R 386/2019-2

    Form of order sought

    The applicant claims that the Court should:

    —

    vary the contested decision and reject the opposition;

    —

    in the alternative, annul the contested decision;

    —

    order EUIPO and the other party to pay the costs incurred in the proceedings before the Second Board of Appeal and in the present proceedings.

    Pleas in law

    —

    infringement of Article 42(2) of Council Regulation (EC) No 207/2009;

    —

    infringement of Article 8(1)(b) of Regulation (EU) 2017/1001 of the European Parliament and of the Council.
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