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2017-08-31

CombiGene: FDA approves a gene therapy product from Novartis for the treatment of acute lymphoblastic leukemia

This is the first ever approval of a gene therapy product in the US
and hence an important milestone for gene therapy as such.

30 August 2017 is a historical day for gene therapy! FDA has just
approved the first gene therapy for the US market. By approving
Kymria from the pharmaceutical company Novartis for certain pediatric
and young adult patients with a form of acute lymphoblastic leukemia
(ALL), they have demonstrated their confidence in the safety and
efficacy of a gene therapy product.

This is most likely the first in a row of approved gene therapies we
could expect over the nearest coming years - both in the US and
Europe.

For further information:
CombiGene AB (publ)
Jan Nilsson, CEO
Phone: +46 (0)704 66 31 63
Email: jan.nilsson@combigene.com

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http://news.cision.com/se/combigene/r/fda-approves-a-gene-therapy-produc...
http://mb.cision.com/Main/12318/2337311/716490.pdf

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