Transgene and ProBioGen Join Forces to Advance Individualized Cancer Vaccine Development
05 November 2024 - 5:30PM
UK Regulatory
Transgene and ProBioGen Join Forces to Advance Individualized
Cancer Vaccine Development
Strasbourg (France), Berlin (Germany),
November 5, 2024, 7:30 a.m. CET—Transgene (Euronext
Paris: TNG), a biotech company that designs and develops
virus-based immunotherapies for the treatment of cancer, and
ProBioGen, a leading CDMO in biologics, vaccines and viral vectors,
announce that the companies have entered into a license
agreement for ProBioGen’s AGE1.CR.pIX® suspension cell
line. This partnership aims to add value by combining
ProBioGen’s specific production technology with the manufacturing
capabilities of Transgene’s individualized cancer vaccine program
and its myvac® platform.
ProBioGen’s AGE1.CR.pIX suspension cell line
showcases innovation and reliability in bioprocessing with a proven
track record and is currently in use for multiple late-stage
clinical trials. Renowned for its high yield and scalability, this
platform enables efficient industrial manufacturing processes,
translating into cost-effectiveness and increased productivity in
manufacturing. Additionally, the AGE1.CR.pIX cell line offers
robust growth and excellent genetic stability to ensure consistent
and reliable production.
“We are delighted to embark on this
collaborative journey with ProBioGen,” said Dr.
Alessandro Riva, CEO of Transgene. “The AGE1.CR.pIX
suspension cell line represents a significant addition to further
expand the manufacturing processes for our individualized cancer
vaccines while we work towards providing patients with tailored
patient-specific therapies against cancer on a larger
scale.”
The partnership between Transgene and ProBioGen
underscores a shared commitment to advancing the field of
individualized medicine and to support manufacturing scalability
and optimization.
“We are thrilled to partner with Transgene
in advancing the frontier of personalized cancer vaccines,”
said Dr. Volker Sandig, CSO of
ProBioGen. “Our collaboration holds immense potential
to impact the personalized vaccine space and to offer new
treatments and hope to cancer patients.”
***
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 (formerly Twitter): @TransgeneSA —
LinkedIn: @Transgene
About ProBioGen
ProBioGen is a Berlin-based specialist for developing and
manufacturing complex therapeutic glycoproteins. Combining both
state-of-the-art development services, based on ProBioGen’s
CHO.RiGHT® expression and manufacturing platform, together with
intelligent product-specific technologies yields biologics with
optimized properties. Rapid and integrated cell line and process
development, comprehensive analytical development and following
reliable GMP manufacturing is performed by a highly skilled and
experienced team. All services and technologies are embedded in a
total quality management system to assure compliance with GMP
standards (EMA/FDA).
ProBioGen has been operational for more than 30 years. At three
locations in Berlin, about 300 employees contribute to the creation
of new therapies in medicine and groundbreaking innovations
worldwide through their creative and meticulous work. ProBioGen’s
growth strategy is driven by the expansion of the service value
chain through organic growth.
ProBioGen’s AGE1.CR.pIX cell line is derived from primary cells of
a duck embryo and was designed to comply with health authority
guidelines and the concept of “defined risk.” It was developed as
an alternative to the use of chicken eggs for large-scale vaccine
production. The AGE1.CR.pIX cell line grows in true suspension and
has been optimized for viral vaccine production and stability and
helps to overcome challenges in vaccine development including the
personalized medicine space. It grows in a commercially available,
chemically defined medium without animal components and is an
excellent host for a variety of different virus strains.
Contacts:
Transgene: |
Media: |
Media: |
MEDiSTRAVA |
Caroline Tosch |
Frazer Hall/Sylvie Berrebi |
Corporate Communication Manager |
+ 44 (0)203 928 6900 |
+33 (0)3 68 33 27 38 |
transgene@medistrava.com |
communication@transgene.fr |
|
|
|
Lucie Larguier |
|
Chief Financial Officer |
|
Nadege Bartoli |
|
IR Analyst and Financial Communications Officer |
|
+33 (0)3 88 27 91 03 /00 |
|
investorrelations@transgene.fr |
|
|
|
ProBioGen: |
Media: |
Dr. Gabriele Schneider |
Sarah Wandrey |
Chief Business Officer |
Senior Communications Manager |
cdmo@probiogen.de |
press@probiogen.de |
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.
- 20241105_-_TransgeneProbiogen_EN
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