A Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients With nAMD

Description

This is a Prospective, Non-interventional, Multicenter, Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients with Neovascular (Wet) Age-related Macular Degeneration (nAMD). All subject who completed the parent clinical study (NCT06213038 and NCT05986864) will undergo safety and efficacy assessments up to 5 years post study drug injection.

Conditions

Neovascular (Wet) Age-related Macular Degeneration

Study Overview

Study Details

Study overview

This is a Prospective, Non-interventional, Multicenter, Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients with Neovascular (Wet) Age-related Macular Degeneration (nAMD). All subject who completed the parent clinical study (NCT06213038 and NCT05986864) will undergo safety and efficacy assessments up to 5 years post study drug injection.

A Prospective, Non-interventional, Multicenter, Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients With Neovascular (Wet) Age-related Macular Degeneration (nAMD)

A Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients With nAMD

Condition
Neovascular (Wet) Age-related Macular Degeneration
Intervention / Treatment

-

Contacts and Locations

Boston

Ophthalmic Consultants of Boston, Boston, Massachusetts, United States, 02114

Katy

Retina Consultants of Texas, Katy, Texas, United States, 77494

Norfolk

Wagner Macula & Retina Center, Norfolk, Virginia, United States, 23502

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * nAMD subjects who have been enrolled in the SKG0106-related study and received SKG0106 injection;
  • * Subjects who voluntarily sign an informed consent form (ICF) and comply with the protocol to complete the study
  • * Subjects who are judged by the investigator unsuitable for this study

Ages Eligible for Study

50 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Skyline Therapeutics,

Study Record Dates

2031-03