LEIDEN, The Netherlands, Oct. 31, 2017 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing lives through the creation of transformative RNA medicines for the treatment of severe genetic rare diseases including cystic fibrosis, Leber's congenital amaurosis 10 and dystrophic epidermolysis bullosa, today announced a presentation at the EuroTIDES conference taking place November 7 – 10, 2017 in Vienna, Austria.
The presentation titled “IPRP UPLC Method Optimization for the Separation of Short- and Longmer Impurities in Oligonucleotide Therapeutics” by Hilde van Hattum, Ph.D., Sr. Scientist Characterisation & BioAnalytics at ProQR will take place on November 9, 2017 at 2:30pm CET. Additional information about the presentation and the EuroTIDES conference is available online.
About ProQR
ProQR Therapeutics is dedicated to changing lives through the creation of transformative RNA medicines for the treatment of severe genetic rare diseases such as cystic fibrosis, Leber’s congenital amaurosis 10 and dystrophic epidermolysis bullosa. Based on our unique proprietary RNA repair platform technologies we are growing our pipeline with patients and loved ones in mind.
*Since 2012*
FORWARD-LOOKING STATEMENTS
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ProQR Therapeutics N.V.:
Media and Investor Contact:
Bonnie Ortega
T: +1 858 245 3983
ir@proqr.com