Transgene and BioInvent to Present Poster on Oncolytic Virus, BT-001, at ESMO 2024
July 22 2024 - 1:00AM
UK Regulatory
Transgene and BioInvent to Present Poster on Oncolytic Virus,
BT-001, at ESMO 2024
Strasbourg, France, and Lund, Sweden, July 22,
2024, 8:00 a.m. CET – Transgene (Euronext Paris:
TNG), a biotech company that designs and develops
virus-based immunotherapies for the treatment of cancer, and
BioInvent International AB (“BioInvent”)
(Nasdaq Stockholm: BINV), a biotech company focused on the
discovery and development of novel and first-in-class
immune-modulatory antibodies for cancer immunotherapy, will
jointly present a poster on initial clinical results from the Phase
I part of the ongoing randomized Phase I/IIa trial of BT-001 at the
European Society of Medical Oncology (ESMO) Annual
Meeting. ESMO will take place in Barcelona, Spain, from September
13 to 17, 2024.
Poster and abstract title: “Initial
clinical results of BT-001, an oncolytic virus expressing an
anti-CTLA4 mAb, administered as single agent and in combination
with pembrolizumab in patients with advanced solid
tumors.”
- Presentation topic: Investigational immunotherapy
- Presentation number: 1024P
- Speaker: Stéphane Champiat
The abstract will be available on ESMO’s website
on September 9, 2024, at 0:05 a.m. CEST.
BT-001 is an oncolytic virus generated using
Transgene’s Invir.IO® platform and its patented large-capacity
VVcopTK-RR- oncolytic virus, which has been engineered to encode
both a Treg-depleting recombinant human anti-CTLA-4 antibody
generated by BioInvent’s proprietary n-CoDeR®/F.I.R.S.T™ platforms,
and the human GM-CSF cytokine.
BT-001 is expected to induce a much stronger and
more effective antitumoral response by selectively targeting the
tumor microenvironment, thereby potentially enhancing the safety
and tolerability profile of the anti-CTLA-4 antibody through
reduced systemic exposure.
The ongoing Phase I/IIa study (NCT04725331) is a
multicenter, open label, dose-escalation trial evaluating BT-001 as
a single agent and in combination with pembrolizumab (anti-PD-1
treatment). Patient inclusions are ongoing in Europe (France,
Belgium) and the trial has been authorized in the US.
***
About Transgene
Transgene (Euronext: TNG) is a biotechnology
company focused on designing and developing targeted
immunotherapies for the treatment of cancer. Transgene’s programs
utilize viral vector technology with the goal of indirectly or
directly killing cancer cells.
The Company’s clinical-stage programs consist of
a portfolio of therapeutic vaccines and oncolytic viruses:
TG4050, the first individualized therapeutic vaccine based on the
myvac® platform, 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.
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 (previously-Twitter): @TransgeneSA -
LinkedIn: @Transgene
About BioInvent
BioInvent International AB (Nasdaq Stockholm: BINV) is a
clinical-stage biotech company that discovers and develops novel
and first-in-class immuno-modulatory antibodies for cancer therapy,
with currently four drug candidates in five ongoing clinical
programs in Phase 1/2 trials for the treatment of hematological
cancer and solid tumors, respectively. The Company’s validated,
proprietary F.I.R.S.T.™ technology platform identifies both targets
and the antibodies that bind to them, generating many promising new
drug candidates to fuel the Company’s own clinical development
pipeline and providing licensing and partnering opportunities.
The Company generates revenues from research collaborations and
license agreements with multiple top-tier pharmaceutical companies,
as well as from producing antibodies for third parties in the
Company’s fully integrated manufacturing unit. More information is
available at www.bioinvent.com. Follow on Twitter: @BioInvent.
More information is available at www.bioinvent.com.
Follow us on Twitter: @BioInvent
Contacts
Transgene
Contact:
Media:
Caroline Tosch
Corporate Communication Manager
+33 3 68 33 27 38
communication@transgene.fr
Investor:
Nadege Bartoli
IR Analyst and Financial Communications Officer
+33 3 88 27 91 03
Lucie Larguier
Chief Financial Officer
+33 3 88 27 91 00
investorrelations@transgene.fr |
Transgene
Media Contact:
MEDiSTRAVA
Frazer Hall/Sylvie Berrebi
+ 44 (0)203 928 6900
transgene@medistrava.com |
BioInvent :
Cecilia Hofvander
Senior Director Investor Relations
+46 (0) 46 286 85 50
cecilia.hofvander@bioinvent.com
Transgene 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.
BioInvent disclaimer
The press release contains statements about
the future, consisting of subjective assumptions and forecasts for
future scenarios. Predictions for the future only apply as the date
they are made and are, by their very nature, in the same way as
research and development work in the biotech segment, associated
with risk and uncertainty. With this in mind, the actual outcome
may deviate significantly from the scenarios described in this
press release.
- 20240722_Transgene_ESMO_curtain_Raiser_BT001_EN
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