PARIS--(BUSINESS WIRE)--Regulatory News:
BioAlliance Pharma SA (Paris:BIO) (Euronext Paris-BIO), a company dedicated to the supportive care and treatment of cancer patients, today announced the award of €2 million in funding over 30 months from the « Fond Unique Interministériel » (a French program supporting collaborative research projects) including an amount of €743,000 specifically allocated to BioAlliance Pharma. This program aims at establishing the proof of concept for the administration by mucosal route of biological products. The first application is a peptide benefiting from the delivery properties of the Lauriad™ mucoadhesive technology.
This program will also permit to test the Lauriad™ technology in the veterinary area.
This collaborative program, co-labelled by both « Clusters of excellence » Medicen Paris Region and Atlanpôle, aims at designing a flu vaccine administered by mucosal route.
The consortium is led by BioAlliance Pharma and involves several academic centers and industrial partners:
- The « Laboratoire de Virologie et Pathologies Humaines VirPath » (Lyon), headed by Pr. Bruno Lina, National flu reference center.
- The « Laboratoire EA 401 Matériaux et Produits de Santé », headed by Pr. Pierre Tchoreloff from Paris XI University, specialized in optimization of peptide formulations.
- Sogeval, a French veterinary drug company, which develops, produces, and markets veterinary products. It has developed a range of pet drugs, particularly in infectiology. The involvement of Sogeval could open the path to new opportunities for the Lauriad™ muco-adhesive technology in the veterinary area.
- Gredeco, founded by Pr. Lofti Ben Slama (Paris), will be in charge of the studies on peptide mucous penetration.
- Pr Pierre Dellamonica’s team, from Nice University Hospital, worldwide known for its expertise in infectiology, will be in charge of immunological assessment prior to entry into clinical phase.
« This program is capitalizing on the Lauriad™ patented mucoadhesive technology, already validated with chemical molecules for Loramyc® and Sitavir®. This substantial public grant will open the path to new application fields with complex biological products and new potential markets”, stated Dominique Costantini, CEO of BioAlliance Pharma.
About BioAlliance Pharma
Dedicated to cancer and supportive
care – cancer related pathologies, chemotherapy and radiotherapy-induced
complications and opportunistic infections in immunocompromised patients
– BioAlliance conceives and develops innovative products, 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; the products’ commercialization rights are licensed to
international commercial partners invested in the hospital setting. In
areas where medical needs are insufficiently met, its targeted
approaches help overcome drug resistance and improve patient health &
quality of life.
BioAlliance Pharma has developed an advanced product portfolio:
Loramyc®/Oravig®
(oropharyngeal candidiasis in immunocompromised patients):
Registered in 26 European countries, in Korea and in the United States
Setofilm®
(prevention and treatment of -chemotherapy, radiotherapy and post
operative- induced nausea and vomiting in adults and children):
Registered in 16 European countries
Sitavir® (Acyclovir
Lauriad TM) (labialis herpes): Positive phase III
final results; registration status
Fentanyl LauriadTM
(chronic cancer pain): Positive preliminary Phase I results
AMEP®
(invasive melanoma): Phase I
Clonidine LauriadTM (mucositis):
Phase II
Doxorubicin Transdrug® (liver cancer): Phase II
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 2009
Reference Document filed with the AMF on June 29, 2010, which is
available on the AMF website (http://www.amf-france.org)
or on BioAlliance Pharma SA's website (http://www.bioalliancepharma.com).