Availability of Preparatory Documents for the Combined General Meeting of May 15, 2025
24 Avril 2025 - 8:00AM
UK Regulatory
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) n° 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® 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® viral
backbone. The Company also conducts innovative discovery and
preclinical work, aimed at developing novel viral vector-based
modalities.
With Transgene’s myvac® platform, therapeutic
vaccination enters the field of precision medicine with a novel
immunotherapy that is fully tailored to each individual. The
myvac® 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®, 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 Manager |
Chief Financial
Officer (CFO) |
+33 (0)3 68 33 27 38 |
Nadege
Bartoli |
communication@transgene.fr |
Investor
Relations Analyst
and Financial Communications 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 (http://www.amf-france.org) or on Transgene’s website
(www.transgene.fr). 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.
Transgene (EU:TNG)
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