BioAlliance Pharma presents preclinical and phase I clinical results with its AMEP biotherapy for metastatic melanoma
Preclinical efficacy and safety results supporting ongoing phase I clinical trial were presented. This latter trial evaluates safety and efficacy of intratumoral electrotransfer of AMEP® biotherapy in patients suffering from advanced or metastatic melanoma. It is being conducted in 3 specialized centers: in Denmark at the Copenhagen University Herlev Hospital, in France at the Gustave Roussy Institute of Villejuif and in Slovenia at the Institute of Oncology of Ljubljana.
Preliminary phase I clinical trial results showed a satisfactory safety and a well accepted electrotransfer technology in the first patients treated with the AMEP® biotherapy.
“These preliminary results confirm the interest of the anti-invasive AMEP® biotherapy in BioAlliance’s clinical programme portfolio; it represents a potential disrupting technology project”, explains Pierre Attali, COO of BioAlliance Pharma, in charge of Strategy and Medical Affairs. “This program is co-financed by OSEO's Strategic Industrial Innovation Programme to the "Cancer Anti-invasive Program" (CAP) consortium, associating the academic research, industrials and melanoma clinicians. This high quality consortium extends the scope of the program to a “companion” markers research, helpful in the follow-up of these severe patients”, adds Dominique Costantini, CEO.
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