Viewing Study NCT06183814



Ignite Creation Date: 2024-05-06 @ 7:56 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06183814
Status: RECRUITING
Last Update Posted: 2024-01-09
First Post: 2023-12-04

Brief Title: A Study of EXG102-031 in Participants With wAMD
Sponsor: Hangzhou Jiayin Biotech Ltd
Organization: Hangzhou Jiayin Biotech Ltd

Study Overview

Official Title: An Open-label Dose-escalation Phase IIIa Study to Evaluate the Safety and Efficacy of EXG102-031 Intraocular Injection in Participants With Neovascular Age-related Macular DegenerationwAMD
Status: RECRUITING
Status Verified Date: 2024-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In neovascular wet age-related macular degeneration wAMD the macula or the part of the eye that provides the clear detailed central vision is being affected by abnormal blood vessel growth and leakage This leakage affects the vision over time and can lead to severe blurriness or blinding EXG102-031 was made to block the extra vessel formation which would lead to less leakage affecting the vision Before EXG102-031 can be tested for its efficacy if it makes vision better it must be tested to see if it is safely tolerated to confirm it can continue to be studied in more patients with wAMD
Detailed Description: Age-related macular degeneration AMD is a major cause of blindness and visual impairment in older adults The wet form of AMD also called neovascular AMD nAMD usually causes faster vision loss than the dry form The most common current treatments of nAMD are products that inhibit vascular endothelial growth factor VEGF including ranibizumab LUCENTIS Genentech and aflibercept EYLEA Regeneron and are delivered by intravitreal injections at 4 to 16 week intervals and continued indefinitely This Open-label Dose-escalation Phase IIIa Study is designed to evaluate the safety and efficacy of EXG102-031 intraocular Injection in participants with wetNeovascular Age-related Macular DegenerationwAMD

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None