Company intelligence / Profile preview
VeonGen Therapeutics
- Ownership
- Private
- Development stage
- Preclinical
Overview
VeonGen’s lead program VG801 is in a first-in-human Phase 1/2 clinical trial for Stargardt disease and has received FDA Rare Pediatric Disease Designation as well as acceptance into the FDA’s Rare Disease Endpoint Advancement pilot program. The company also has a second clinical-stage program, VG901 for retinitis pigmentosa caused by CNGA1 mutations. Both programs are enabled by proprietary gene delivery platforms designed to overcome limitations of current AAV-based therapies[1][5][6].
- Therapeutic areas
- Ophthalmology
- Modalities
- Gene therapyAdeno-associated virus (AAV)-based gene therapyDual AAV gene therapy
- Industry
- Biotech
Drug pipeline
5 assets4 more assets in the full pipeline.
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