LEIDEN, Netherlands & CAMBRIDGE, Mass., April 02, 2021 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing lives through the creation of transformative RNA therapies for
LEIDEN, Netherlands & CAMBRIDGE, Mass., April 23, 2021 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing lives through the creation of transformative RNA therapies for
… to changing lives through the creation of transformative RNA therapies for severe genetic rare diseases, today … QR-421a QR-421a is a first-in-class investigational RNAtherapy designed to address the underlying cause of vision …
… to changing lives through the creation of transformative RNA medicines for severe genetic rare diseases, today … in 2021. “From previous clinical trials we have seen that RNA therapies can be a promising approach for patients with … excited to have started a clinical trial for the third RNAtherapy in our inherited retinal disease pipeline.” About the …
… to changing lives through the creation of transformative RNA medicines for the treatment of severe genetic rare … lead to blindness in early childhood. No form of therapy is currently available,” said Dr. Katarina Stingl of … Tübingen, Investigator in the ILLUMINATE trial. “ProQR’s RNAtherapy for the p.Cys998X mutation showed the potential …
… to changing lives through the creation of transformative RNA medicines for the treatment of severe genetic rare … first studies of its kind exploring the impact of ProQR’s RNA therapies on patients with Usher syndrome due to an Exon … STELLAR trial will explore whether QR-421a (ProQR’s RNAtherapy) can slow disease progression or even reverse it. …
… ProQR to Present at the Retinal Cell and Gene Therapy Innovation Summit and the Association for Research in … to changing lives through the creation of transformative RNA therapies, today announced several presentations at the …