Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06461286
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-14
First Post:
2024-06-05
Brief Title:
SAD of IVT PYC-001 in OPA1 Mutation-Associated Autosomal Dominant Optic Atrophy Sundew
Sponsor:
PYC Therapeutics
Organization:
PYC Therapeutics
Conditions & Keywords Data
Conditions:
| Name |
|---|
| Kjer Optic Atrophy |
| OPA1 Gene Mutation |
| Autosomal Dominant Optic Atrophy |
| Hereditary Optic Atrophies |
Keywords: