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-0.0344827586206895 -0.0344827586206895 -0.0172413793103448 -0.0172413793103448 0.0172413793103449 0.0172413793103449 0.0431034482758622 0.0517241379310346
Stock impact report

Foundation Fighting Blindness will provide up to $7.5 million in funding to develop ProQR’s candidate QR-421a for Usher syndrome type 2A

ProQR Therapeutics N.V. - Ordinary Shares (PRQR) 
Last proqr therapeutics n.v. - ordinary shares earnings: 2/26 07:00 am Check Earnings Report
US:NASDAQ Investor Relations: proqr.com
Company Research Source: GlobeNewswire
Foundation Fighting Blindness and ProQR enter into a partnership to develop QR-421a for Usher syndrome type 2A, targeting mutations in exon 13 of the causative USH2A gene. Foundation Fighting Blindness will provide milestone-based co-funding of up to $7.5 million to ProQR to advance the program into the clinic. QR-421a received orphan drug designation from the FDA. There are currently no therapies commercially available or in clinical development for the vision loss associated with Usher syndrome type 2A.QR-421a is part of ProQR’s growing ophthalmology pipeline which also includes lead candidate, QR-110 for Leber’s congenital amaurosis 10 currently in clinical trials, and three additional pipeline programs, QR-411 that addresses another genetic mutation resulting in Usher syndrome type 2A, QRX-1011 for Stargardt’s disease and QRX-504 for Fuchs endothelial corneal dystrophy.  QR-421a is expected to advance towards the clinic in 2018, with clinical data expected in 2019. COLUMBIA, Md. Show less Read more
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