Open-Label, Single-Dose, Exploratory Study With QR-504a to Evaluate Safety, Tolerability, and Corneal Endothelium Molecular Biomarker(s) in Subjects With Fuchs Endothelial Corneal Dystrophy With Trinucleotide Repeat Expansion in the TCF4 Gene (FECD3)
Latest Information Update: 21 May 2022
At a glance
- Drugs QR-504a (Primary)
- Indications Fuchs' endothelial dystrophy
- Focus Adverse reactions; First in man; Proof of concept; Therapeutic Use
- Acronyms Fuchs Focus
- Sponsors ProQR Therapeutics
Most Recent Events
- 05 May 2022 Status changed from recruiting to withdrawn prior to enrolment. Reason the study was stopped: No patients.
- 18 Nov 2021 According to a ProQR Therapeutics media release, the company present data of this study at the Analyst Event via webcast.
- 05 Aug 2021 Status changed from planning to recruiting, according to a ProQR Therapeutics media release.