The last years were very promising for gene therapeutic approaches. A number of successful treatments of cancer or rare diseases were reported, as well as FDA approval of first gene therapeutic products. Until now, these pioneering treatments have been used primarily when conventional therapies reach their limits. Development, manufacturing, quality control and clinical application of gene therapeutic products are very challenging – and still far from routine.
The conference addresses the major issues on the way to save and successful products: “Gene Therapy – Ready for the Market?”
Manufacturing and quality control of gene therapeutic products
Genome editing for gene therapy development
Development and manufacturing of gene transfer vectors
Manufacturing of cell-based gene therapeutic products
Viral vectors for vaccination
Clinical applications of gene therapeutic products
Regulatory pathways to enable gene therapy
Confirmed Keynote Speakers:
Christian J. Buchholz, Paul-Ehrlich-Institut, Langen/D
Hildegard Büning, Hannover Medical School, Hannover/D
John Campbell, Scottish National Blood Transfusion Center, Edinburgh/UK
Klaus Cichutek, Paul-Ehrlich-Institut, Langen/D
Markus Hörer, Freeline Therapeutics GmbH, Planegg-Steinkirchen/D
Amine Kamen, McGill University, Montreal/CAN
Ulrike Köhl, Fraunhofer-Institut für Zelltherapie und Immunologie IZ, Leipzig/D
Otto Merten, Genethon, Evry/F
Axel Schambach, Hannover Medical School, Hannover/D
Information on participating / attending:
You are most welcome to contribute to the conference programme and submit your paper until 03 September 2018.
01/30/2019 - 02/01/2019
60486 Frankfurt am Main
Business and commerce, Scientists and scholars
Types of events:
Conference / symposium / (annual) conference
Dr. Kathrin Rübberdt
Event is free:
Language of the text:
URL of this event: http://idw-online.de/en/event61107
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