REGENXBIO, Inc.

Coming – October 6

A Biotech Powerhouse With 3 Blockbuster Opportunities

Date and Time

October 6

12:00 PM ET / 9:00 AM PT

Details will be provided upon RSVP approval

About this Event

Regenxbio [NASDAQ: RGNX] has three assets in pivotal trials that are set to reach critical milestones this year. Regenxbio is currently targeting Hunter Syndrome, Duchenne Muscular Dystrophy, and Chronic Retinal Disease with treatments that have the potential to become standard of care in markets worth a total of $26B.

The company recently announced new, positive data from their pivotal trial of RGX-121 providing further evidence of its long-term potential to improve the trajectory of Hunters syndrome for boys with this devastating, degenerative disease. Currently there is no treatment for Hunter syndrome.

In addition to its three late-stage clinical assets, Regenxbio is differentiated from other gene therapy companies in several ways:
  • They are one of a few gene therapy companies worldwide with a cGMP facility capable of producing at commercial scale.
  • They already have partnerships with global pharmaceutical companies including Abbvie, Nippon Shinyaku, and Novartis.
  • Their NAV Platform technology is capable of developing broad applications across multiple disease states, creating a robust pipeline of future opportunities.
  • Their Hunter Syndrome program has received a Priority Review Voucher worth $150M.
Register now to join this 30-minute webinar with George McDougal, head of investor relations for Regenexbio, to hear more about the company’s unique approach to gene therapy, and how their treatments have the potential to become standard of care in markets worth a total of $26B.

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