Get the full list », You’re viewing 5 of 19 investors. Our initial product candidate, AVXS-101, is our proprietary gene therapy product candidate currently in development for the treatment of spinal muscular atrophy, or SMA, Type 1, the leading genetic cause of infant mortality, and for the treatment of SMA Type 2. This process is automatic. Developer of gene therapies designed to treat rare and orphan neurological genetic diseases. ... also spent a considerable part of 2019 dealing with data-integrity concerns which emerged from its 2018 buyout of AveXis, the gene-therapy maker Novartis had acquired for US$ 8.7 billion. Ut enim ad minim veniam, quis nostrud exercitation u. ng elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. In addition to developing AVXS-101 to treat SMA Type 1 and Type 2, we also plan to develop other novel treatments for rare neurological diseases, including Rett syndrome (RTT) and a genetic form of amyotrophic lateral sclerosis (ALS) caused by mutations in the superoxide dismutase 1 (SOD1) gene. Personalize which data points you want to see and create visualizations instantly.

REGENXBIO is headquartered in Rockville, Maryland, and was founded in 2009. Get the full list », You’re viewing 2 of 10 board members. AveXis 's estimated annual revenue is currently $203.2M per year.AveXis; received $460.0M in venture funding in January 2018.AveXis 's estimated revenue per employee is $155,000AveXis 's total funding is $170.5M.

AveXis, Inc. is a clinical-stage gene therapy company dedicated to developing and commercializing novel treatments for patients suffering from rare and life-threatening neurological genetic diseases. AveXis was founded in 2010.. Who are AveXis key executives?. Email: info@avexis.com AveXis.

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Bannockburn, IL 60015

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