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    Allergan Acquires Gene Therapy Company RetroSense Therapeutics

    Pia Rivera
    Sep. 06, 2016 10:09AM PST
    Life Science Investing News

    Allergan plc (NYSE:AGN) has acquired RetroSense Therapeutics LLC, a private, clinical-stage biotechnology company focused on novel gene therapy approaches to restore vision in patients suffering from blindness. Under the terms of the transaction, Allergan has paid RetroSense a $60 million upfront payment. As quoted in the press release: “The acquisition of RetroSense and its RST-001 …

    Allergan plc (NYSE:AGN) has acquired RetroSense Therapeutics LLC, a private, clinical-stage biotechnology company focused on novel gene therapy approaches to restore vision in patients suffering from blindness. Under the terms of the transaction, Allergan has paid RetroSense a $60 million upfront payment.
    As quoted in the press release:

    “The acquisition of RetroSense and its RST-001 program builds on Allergan’s deep commitment to eye care, and our focus on investing in game-changing innovation for retinal conditions, including Retinitis Pigmentosa, where patients desperately need treatment options,” said Brent Saunders, CEO and President of Allergan.
    Retinitis Pigmentosa (RP) is a group of rare, inherited genetic disorders characterized by progressive peripheral vision loss and night vision difficulties followed by eventual central vision loss and blindness in many cases. Approximately 100,000 people living in the USi and 14 to 33 per 100,000 people worldwide have the disorder.ii
    RST-001 is first-in-class gene therapy application of optogenetics, a therapeutic approach that confers light sensitivity to cells that were not previously, or natively, light sensitive. By applying optogenetics to retinas in which rod and cone photoreceptors have degenerated, the technology introduces additional light sensitivity to the retina. In 2014, RST-001 received an Orphan Drug Designation by the US FDA for the treatment of Retinitis Pigmentosa.

    Click here for the full press release.

    brent saundersorphan drug designationorphan drug
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