Availability of Preparatory Documents for the Combined General Meeting of May 15, 2025

Strasbourg, France, April 24, 2025, 8:00 a.m. CET - Transgene (Euronext Paris: TNG), a biotech company that designs and develops virus-based immunotherapies, announced that the documentation related to the Combined General Meeting (ordinary and extraordinary sessions) of Transgene's shareholders is available.

The notice of meeting, comprising the agenda and the draft resolutions, was published in the Bulletin des Annonces Légales Obligatoires (BALO) ndeg 42 of April 7, 2025 and in the corrigendum no. 47 of April 18, 2025.

These notices include information on how to attend and vote at the General Meeting.

The General Meeting will be held on May 15, 2025, at 10:00 am CET, at the Company's headquarters in Illkirch-Graffenstaden (France). It will be broadcast live on the Company's website (www.transgene.fr under "Investors - Shareholders' Meeting") and the video will also be available later within the time period provided for by the regulations.

The procedures and rules relative to the holding of this shareholder meeting, as well as the exercise of the right to request documents and submit written questions, are set out in the notice of meeting published on April 7, 2025 and are also posted at www.transgene.fr/AG2025.

About Transgene

Transgene (Euronext: TNG) is a biotechnology company focused on designing and developing targeted immunotherapies for the treatment of cancer. The Company's clinical-stage programs consist of a portfolio of viral vector-based immunotherapeutics. TG4050, the first individualized therapeutic vaccine based on the myvac$(R)$ platform is the Company's lead asset, with demonstrated proof of principle in patients in the adjuvant treatment of head and neck cancers. The portfolio also includes other viral-vector-based immunotherapies: TG4001 for the treatment of HPV-positive cancers, as well as BT-001 and TG6050, two oncolytic viruses based on the Invir.IO(R) viral backbone. The Company also conducts innovative discovery and preclinical work, aimed at developing novel viral vector-based modalities.

With Transgene's myvac(R) platform, therapeutic vaccination enters the field of precision medicine with a novel immunotherapy that is fully tailored to each individual. The myvac(R) approach allows the generation of a virus-based immunotherapy that encodes patient-specific mutations identified and selected by Artificial Intelligence capabilities provided by its partner NEC.

With its proprietary platform Invir.IO(R), Transgene is building on its viral vector engineering expertise to design a new generation of multifunctional oncolytic viruses.

Additional information about Transgene is available at: www.transgene.fr

Follow us on social media: X (formerly Twitter): @TransgeneSA -- LinkedIn: @Transgene

Contacts

 
   Media:                                        Investors & Analysts: 
   Caroline Tosch                                    Lucie Larguier 
   Corporate and Scientific Communications      Chief Financial Officer 
    Manager                                               $(CFO.AU)$ 
   +33 (0)3 68 33 27 38                              Nadege Bartoli 
                                               Investor Relations Analyst 
                                              and Financial Communications 
   communication@transgene.fr                            Officer 
   MEDiSTRAVA                                       +33 (0)3 88 27 91 00/03 
   Frazer Hall/Sylvie Berrebi                investorrelations@transgene.fr 
   + 44 (0)203 928 6900 
   transgene@medistrava.com 
 

Disclaimer

This press release contains forward-looking statements, which are subject to numerous risks and uncertainties, which could cause actual results to differ materially from those anticipated. The occurrence of any of these risks could have a significant negative outcome for the Company's activities, perspectives, financial situation, results, regulatory authorities' agreement with development phases, and development. The Company's ability to commercialize its products depends on but is not limited to the following factors: positive pre-clinical data may not be predictive of human clinical results, the success of clinical studies, the ability to obtain financing and/or partnerships for product manufacturing, development and commercialization, and marketing approval by government regulatory authorities. For a discussion of risks and uncertainties which could cause the Company's actual results, financial condition, performance or achievements to differ from those contained in the forward-looking statements, please refer to the Risk Factors ("Facteurs de Risque") section of the Universal Registration Document, available on the AMF website . Forward-looking statements speak only as of the date on which they are made, and Transgene undertakes no obligation to update these forward-looking statements, even if new information becomes available in the future.

Attachment

   -- 20250424_document_AG_EN 

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April 24, 2025 02:00 ET (06:00 GMT)