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Funded Projects › FP7

MABTOX · Generation and Evaluation of ""Next-generation"" Antibody-Toxin-Conjugates for Cancer Therapy""

FP7Status: CLOSED1 October 201331 December 2015EU funding €1,061,000

Therapeutic antibodies have transformed cancer therapy during the last decade, due to their high selectivity of targeting cancer cells in comparison to standard small molecule chemotherapy. Most recently, the coupling of cellular toxins to therapeutic antibodies has demonstrated an even greater efficacy in the therapy of cancer and the first, highly potent antibody drug conjugate (ADC), Adcetris®, was FDA approved in August 2011.All ADCs currently in clinical development are generated by chemical conjugation of small molecule toxins to antibodies. This is an inefficient process, as site and ratio of toxin coupling cannot be controlled. In addition, the chemical conjugation involves chemical modification of potentially functional parts of the antibody. This can have negative effects on stability, specificity, CMC properties and the overall structure of the antibody. All this renders ADC manufacturing highly challenging, complicates regulatory procedures, and adds to development time and costs.The SME consortium has complementary proprietary technologies and proposes to leverage this complementary expertise and know-how for defining novel processes of enzymatically conjugating small molecule toxins to antibodies that allow full control about toxin coupling site and ratio. Due to the high selectivity of enzymatic conjugation and physiologic conjugation conditions, it is expected that more homogeneous ADCs are generated with better CMC properties, higher potency, and at lower cost-of-goods in manufacturing. The consortium members believe that this represents a disruptive technology that will be highly competitive to traditional chemical conjugation, currently dominated by U.S.-based ADC technology companies Seattle Genetics and Immunogen. In addition to novel composition-of-matter IP, important novel know-how for ADC development will be created. Most importantly, better quality and potency of these “next-generation” ADCs will eventually benefit cancer patients.

Consortium · 12 organisations

coordinator

NBE-THERAPEUTICS AG

CH · €422,380

participant

BIOMEDAL SL

ES · €8,800

participant

ERA BIOTECH

ES · €171,758

participant

JPT PEPTIDE TECHNOLOGIES GMBH

DE · €8,800

participant

INNO TUNE BVBA

BE · €9,040

participant

TBD-BIODISCOVERY OU

EE · €7,590

participant

ZERA INTEIN PROTEIN SOLUTIONS SL

ES · €112,677

participant

CHARLES RIVER DISCOVERY RESEARCH SERVICES GERMANY GMBH

DE · €12,760

participant

PROTAGEN PROTEIN SERVICES GMBH

DE · €16,040

participant

EVITRIA AG

CH · €14,540

participant

Westfälische Wilhelms-Universität Münster

DE

participant

TUBE PHARMACEUTICALS GMBH

AT · €276,615

Research fields

View the official record on CORDIS →

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Source: CORDIS, Publications Office of the European Union. Global Research Partnerships surfaces open EU research data to help you find collaborators; we are not affiliated with the European Union.