Regulatory News:
BioAlliance Pharma SA (Paris:BIO) (Euronext Paris - BIO), a company
dedicated to specialty and orphan pharma products in oncology and
supportive care, today announced a half-day symposium:
"Oncology: key issues for the future"
On March 20, 2012 (from 9 am to 12 midday)
During the morning symposium, fund managers, analysts and media
representatives will be invited to listen to and discuss with
international leading specialists:
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Bertrand Vergely, Philosopher
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Pr. David Khayat, Professor in Oncology, La Pitié-Salpêtrière
Hospital (Paris, France)
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Pr. Philippe Merle, Professor in Hepatology, La Croix Rousse
Hospital (Lyon, France)
-
Pr. Michael Henke, Professor in Radiotherapy, Universitätsklinikum
Freiburg (Freiburg, Germany)
BioAlliance Pharma will be represented by:
-
Judith Greciet, Chief Executive Officer
-
Pierre Attali, Chief Operating Officer, Strategy and Medical Affairs
The event will take place at BioAlliance Pharma's head office (in Paris)
on Tuesday, March 20, 2012, from 9am onwards (by invitation only). The
final morning's program will be soon announced.
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; 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:
Specialty products
Loramyc®/Oravig®
(oropharyngeal candidiasis in immunocompromised patients): Registered in
28 countries (EU, US, Korea)
Sitavir® (Acyclovir LauriadTM)
(labialis herpes): Positive phase III final results; registration status
Fentanyl
LauriadTM (chronic cancer pain): Positive preliminary Phase I
results
Orphan Oncology products
Livatag® (Doxorubicin
Transdrug™) in primary) liver cancer: Authorization for Phase III
clinical trial
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 2010 Reference Document filed with
the AMF on April 7, 2011, which is available on the AMF website (http://www.amf-france.org)
or on BioAlliance Pharma SA's website (http://www.bioalliancepharma.com).
