BioAlliance Pharma Signs a Collaborative Agreement with One of the Worldwide Leaders in Vaccines for a Vaccine Application of...
01 March 2013 - 4:57AM
Business Wire
Regulatory News:
BioAlliance Pharma SA (Euronext Paris - BIO), an innovative
Company dedicated to the development of orphan oncology products
and to supportive care products, announces a collaboration
agreement with one of the world leading vaccine companies to
develop a vaccine application of its Lauriad® mucoadhesive
technology. The terms of this agreement are not disclosed at this
time.
This research program aims at establishing the feasibility of
using Lauriad® technology for vaccination, leading to an efficient
needle-free administration based on the application to the gum of
this mucoadhesive tablet containing a vaccine antigen. Moreover,
this would also avoid the constraints related to manufacturing
sterile injectable forms.
This project is carried out within the Fluriad™ consortium set
in March 2011, co-labeled by both “Clusters of excellence” Medicen
Paris Region and Atlanpôle Biotherapies and financed up to €2
million by the “Fond Unique Interministériel” (a French program
supporting collaborative research projects).
“This collaboration with one of the world leading vaccine
companies shows the potential interest of our innovative Lauriad®
system for a needle-free vaccination. This is also a major step
taken to increase the value of our proprietary Lauriad® technology,
already validated through three major products of our portfolio:
Loramyc® and Sitavig®, already registered, and Validive®, in phase
II clinical development,” stated Judith Greciet, CEO of BioAlliance
Pharma. “A first successful feasibility would open the way to
promising new opportunities in vaccine field with significant
market potential worldwide.”
About BioAlliance Pharma
Dedicated to cancer and supportive care treatment with a focus
on resistance targeting and orphan products, BioAlliance conceives
and develops innovative products, for specialty markets especially
in the hospital setting and for orphan or rare diseases.
Created in 1997 and introduced to the Euronext Paris market in
2005, BioAlliance Pharma’s ambition is to become a leading player
in these fields by coupling innovation to patient needs. The
company’s teams have the key competencies required to identify,
develop and register drugs in Europe and the USA.
BioAlliance Pharma has developed an advanced product
portfolio:
Specialty products
Loramyc®/Oravig® (oropharyngeal candidiasis in immunocompromised
patients): Registered in 28 countries (EU, US, Korea)
Sitavir®/Sitavig® (Acyclovir LauriadTM) (labialis herpes):
Registered in 8 European countries, registration status in the
US
Fentanyl LauriadTM (chronic cancer pain): Positive preliminary
Phase I results
Orphan Oncology products
Livatag® (Doxorubicin Transdrug™) (primary liver cancer): Phase
III on going
Validive® (Clonidine LauriadTM) (mucositis): Phase II on
going
AMEP® (invasive melanoma): Phase I on going
For more information, visit the BioAlliance Pharma web site at
www.bioalliancepharma.com
Disclaimer
This communication expressly or implicitly contains certain
forward-looking statements concerning BioAlliance Pharma SA and its
business. Such statements involve certain known and unknown risks,
uncertainties and other factors, which could cause the actual
results, financial condition, performance or achievements of
BioAlliance Pharma SA to be materially different from any future
results, performance or achievements expressed or implied by such
forward-looking statements. BioAlliance Pharma SA is providing this
communication as of this date and does not undertake to update any
forward-looking statements contained herein as a result of new
information, future events or otherwise.
For a discussion of risks and uncertainties which could cause
actual results, financial condition, performance or achievements of
BioAlliance Pharma SA to differ from those contained in the
forward-looking statements, please refer to the Risk Factors
("Facteurs de Risque") section of the 2011 Reference Document filed
with the AMF on April 24, 2012, which is available on the AMF
website (http://www.amf-france.org) or on BioAlliance Pharma SA's
website (http://www.bioalliancepharma.com).
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