The FDA has cleared an investigational new drug application for QR-1123, an investigational oligonucleotide treatment candidate for vision loss with autosomal dominant retinitis pigmentosa due to the P23H mutation in the rhodopsin gene, according to a press release from ProQR Therapeutics.
ProQR’s retinitis pigmentosa candidate gets investigational NDA clearance
By Michael Tattory|
2019-08-13T11:01:13-04:00
August 12th, 2019|News|Comments Off on ProQR’s retinitis pigmentosa candidate gets investigational NDA clearance