ProQR Announces Closing of Underwritten Public Offering of Ordinary Shares with Full Exercise of Underwriters’ Option to Purchase Additional Shares Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … avril 05, 2021
ProQR Appoints Naveed Shams, MD, PhD as Chief Scientific Officer Press release … for the treatment of genetic eye diseases such as Leber congenital amaurosis 10, Usher syndrome and autosomal … octobre 05, 2020
ProQR Announces $30 Million Strategic Convertible Debt Financing Agreement with Pontifax Ventures Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … juillet 14, 2020
ProQR Prices $90 Million Underwritten Public Offering of Ordinary Shares Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … mars 31, 2021
ProQR Announces Proposed Underwritten Public Offering of Ordinary Shares Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … mars 30, 2021
ProQR to Present Results from Phase 1/2 Trial of QR-421a for Usher Syndrome Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … mars 17, 2021
ProQR Strengthens Scientific Advisory Board with Leaders in Inherited Retinal Disease and RNA Therapy Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … juillet 21, 2020
ProQR Appoints Theresa Heggie as Chief Commercial Officer Press release … with a focus on inherited retinal diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … octobre 04, 2021
ProQR Announces Expert Perspectives Call on Disease Education and Endpoints in Usher Syndrome Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … février 16, 2021
ProQR Appoints John Maraganore, PhD, as Strategic Advisor to the Supervisory Board Press release … for the treatment of severe genetic rare diseases such as Leber congenital amaurosis 10, Usher syndrome and retinitis … mars 07, 2022
