Press Releases

Consolidated accounts for the first semester of 2011 And recent significant key events

• Key achievements in the clinical development of orphan oncology products • Strongly reinforced cash position after successful capital increase in August, aiming to finance R&D programs • Optimization of international commercial partnerships with Loramyc® in the development of the leader orphan oncology product Livatag®: The presentation of positive phase II results showing a doubled median survival when compared with…read more →

BioAlliance Pharma announces positive preliminary phase I clinical results with its AMEP® biotherapy for metastatic melanoma

BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today announced preliminary phase I clinical results with its AMEP® biotherapy developed in advanced or metastatic melanoma, an invasive skin cancer of bad prognosis. The objectives of this first phase I trial were to evaluate the safety of intratumoral electrotransfer of AMEP® biotherapy and…read more →

BioAlliance Pharma announces 2 key decisions green light granted from french agency for Livatag® phase |||

Full us rights regained for oravig® BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today announces: • Following PAR Strativa restructuring and change of strategy including recent acquisition of generic portfolio, BioAlliance Pharma has decided to regain full US commercialization rights for Oravig®. The transfer, with no significant impact on BioAlliance Pharma…read more →

Presentation of Livatag® survival results at the international liver cancer congress in Hong Kong

BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today announces oral communication of the Phase II clinical trial results of its orphan product Livatag® at the annual congress of ILCA (International Liver Cancer Association), the only international organization devoted exclusively to liver cancer research with participation of worldwide best specialists. Pr. Philippe…read more →

BioAlliance Pharma initiates the clinical batches production of Livatag® (doxorubicin Transdrug™) for its phase III clinical trial

BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today announces the initiation of the clinical batches production of Livatag® (doxorubicin Transdrug™) for its phase III clinical trial in primary liver cancer. This production will be performed by qualified companies for injectable cytotoxic products in nanoparticle form. The BioAlliance Pharma’s team specialized in…read more →

Q2 2011: BioAlliance Pharma accelerates the progress of its “Orphan oncology products” portfolio and pursues its international partnerships on its “Specialty products”

BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today reported a consolidated turnover of €576,000 for the second quarter of 2011. This turnover is mainly made of recurring revenues from Loramyc®/Oravig®. It also comprises an amount of €113,000 corresponding to the staggering of the upfront payment received from BioAlliance new partner Sosei,…read more →

Successful capital increase for BioAlliance Pharma

Over-subscribed transaction €16.64 million raised (Offering notice number 11-280 dated 30th June 2011 approved by the French financial market regulator AMF) BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan oncology products, today announces its successful capital increase, with maintenance of preferential subscription rights launched on July 1st, 2011, for a total of €16,64 million…read more →

BioAlliance Pharma submits application for orphan medicinal product designation for clonidine Lauriad™ in Europe and the United States

BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to the supportive care and treatment of cancer patients, today announced the submission to the European (EMA) and American (FDA) Drug Agencies of an application for orphan medicinal product designation for clonidine Lauriad™, in the prevention of radiotherapy-induced oral mucositis in patients with head and neck cancer. Clonidine Lauriad™, presently…read more →

BioAlliance Pharma strengthens its proprietary technologies with the grant of its Lauriad™ patents in Asia and with the transfer of Setofilm® back to APR Applied Pharma Research SA, the owner of the technology

BioAlliance Pharma SA (Euronext Paris –BIO), a company dedicated to the supportive care and treatment of cancer patients, today announced the grant of patents protecting its delivery technology Lauriad™ in China and Japan. This delivery technology specifically covers its advanced Specialty products: Loramyc® in the treatment of oropharyngeal candidiasis and Sitavir® in herpes labialis. “After Europe and the US, these…read more →

BioAlliance Pharma filed an appeal to the French Supreme Court contesting a preliminary procedural decision on jurisdiction in the arbitration against SpePharm and SpeBio

The proceedings to the arbitral tribunal are still at a preliminary stage concerning the scope of its jurisdiction. This tribunal will have to rule on the relief sought by BioAlliance Pharma and the counterclaims of SpePharm and SpeBio. BioAlliance Pharma announces today that it has filed an appeal to the French Supreme Court on a procedural matter in this arbitral…read more →

A new Chief Executive Officer to strengthen BioAlliance Pharma’s growth

BioAlliance Pharma SA (Euronext Paris –BIO), a company dedicated to the supportive care and treatment of cancer patients, today announced the appointment of Judith Greciet as Chief Executive Officer, succeeding to Dominique Costantini, co-foundator and Chief Executive Officer, to be effective after the General Assembly Meeting of June 29, 2011. Judith Greciet, PharmD, serves as Chief Operating Officer for BioAlliance…read more →

Combined Ordinary and Extraordinary General Meeting on June 29th 2011

Procedures for obtaining preparatory documents BioAlliance Pharma’s shareholders are invited to attend the Combined Ordinary and Extraordinary General Meeting to be held at 2.00 pm on June 29th 2011 at the company’s head office (49 Boulevard du Général Martial Valin, F-75015 Paris, France). The official notice of the Meeting will be published in the French Republic’s Bulletin des Annonces Légales…read more →

Board evolution at BioAlliance Pharma To support its growth strategy

BioAlliance Pharma’s (Euronext Paris –BIO) Board has approved the draft resolutions on Board changes, to be voted at the General Assembly Meeting on June 29, 2011. Following Mr. André Ulmann and Mr. Gilles Marrache expressed wishes not to pursue their board mandate due to personal constraints, the Board thanks them for their commitment and contribution to its work and will…read more →

BioAlliance Pharma announces that Therabel launches Loramyc®

in Germany with the support of Hikma BioAlliance Pharma SA (Euronext Paris – BIO), a company dedicated to specialty and orphan pharma products in oncology and supportive care, today announced that Loramyc® has been launched in Germany by its European partner Therabel. Therabel has created a fully dedicated team and has also entered into a co-promotion agreement with Hikma Pharma…read more →