ProQR doses first patients in late-stage QR-421a trial for retinitis pigmentosa, Usher syndrome
December 16th 2021The company anticipates that the Sirius and Celeste studies will further validate QR-421a’s ability to stabilize vision loss in people with USH2A mediated retinitis pigmentosa and Usher syndrome.
AcuFocus receives Approvable Letter from FDA for small aperture IOL
December 7th 2021The company will begin commercialization of the IC-8 small aperture IOL, used for cataract patients, upon successful completion of the manufacturing facility inspections and receipt of an official approval order from the FDA, which the company estimates in Q2 2022.