Transgene . (NASDAQ:TRGNY)
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Transgene Manufactures Clinical Lots of HIV Vaccine Candidates
for the EUROVAC Project
STRASBOURG, France, July 1 /PRNewswire-FirstCall/ -- Transgene (Nasdaq: TRGNY;
Nouveau Marche: FR0005175080) today announced that it manufactured clinical
lots of HIV vaccine candidates in the frame of EUROVAC (European Vaccine Effort
against HIV/AIDS), a European cluster of 21 laboratories, funded since 2000 by
the European Union under the 5th Framework Programme.
Partners of EUROVAC, the Karolinska Institutet and Aventis Pasteur, recognizing
Transgene's know-how in the field of recombinant vaccines production, selected
the company to produce clinical lots of NYVAC-based vaccines carrying genes of
HIV-1. Production was completed in Transgene's manufacturing facility located
near Strasbourg, through adaptation of its own MVA manufacturing process to the
production of NYVAC-based products. NYVAC and MVA are both attenuated strains
of the vaccinia virus.
"We are very proud of the confidence put in us by the Karolinska Institutet,
EUROVAC and Aventis Pasteur for our manufacturing capabilities of recombinant
vaccines," stated Jean-Francois Carmier, Chief Executive Officer of Transgene.
"We believe manufacturing contracts add value to our expertise, while
contributing to reducing our burn rate."
About Transgene
Transgene, based in Strasbourg, France, is a biopharmaceutical company
dedicated to the discovery and development of therapeutic vaccines,
immunotherapy products, and delivery technologies for the treatment of diseases
for which there is no cure or adequate treatment at present, with a focus on
the treatment of cancer. Transgene has five products in clinical development,
two of which are in Phase II clinical trials, two in Phase I/II and one that
has completed Phase I clinical trial. Transgene's proprietary vector technology
platform consists of adenovirus and poxvirus.
This press release contains forward-looking statements, including statements
regarding Transgene manufacturing capabilities. Statements that are not
historical facts are based on Transgene's current expectations, beliefs,
estimates, forecasts and assumptions, including Transgene's expectations
related to the reproducibility in humans of the preclinical results, progress
in the clinical trials and Transgene's belief as to the potential to
successfully manufacture products for the effective treatment of illness. The
statements contained in this release are not guarantees of future performance
and involve certain risks, uncertainties and assumptions which are difficult to
predict. Accordingly, actual outcomes and results may differ materially from
what is expressed in those forward-looking statements. Important factors which
may affect Transgene's future operating results include the following:
Transgene's product candidates may not demonstrate therapeutic efficacy after
initial promising results, Transgene may be unable to obtain regulatory
approval for its product candidates, Transgene may be unable to conduct its
clinical trials as quickly as it has predicted, Transgene's clinical trials may
not produce results sufficient to justify further product development,
Transgene may not have sufficient resources to complete the research,
manufacturing and commercialization of any of its product candidates,
competitors may develop technologies or products superior to Transgene's
technologies or products, Transgene may not be able to successfully enforce the
intellectual property rights in all jurisdictions relating to its product
candidates and other important factors described in Transgene's Annual Report
on Form 20-F for the year ended December 31, 2003 filed with the U.S.
Securities and Exchange Commission, including those factors described in the
section entitled "Risk Factors."
DATASOURCE: Transgene
CONTACT: Michel Hubert, VP Business Development, Transgene,
+33-3-88-27-91-12; Michael Long, Cohn & Wolfe, +1-212-798-9775; Estelle
Guillot-Tantay, +33-1-53-70-74-93, or Laurence Heilbronn, +33-1-53-70-74-64,
both of Image 7, for Transgene