Status and phase
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About
This is a clinical study to evaluate the safety, preliminary efficacy, immunogenicity of SKG0106 in subjects with nAMD.
Enrollment
Sex
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Volunteers
Inclusion criteria
Voluntary and able to sign a dated ICF prior to any study-related procedures and able to complete the study as required by the protocol;
Aged ≥ 50 years at screening;
Study Eye:
Diagnosis of nAMD as determined by the PI;
Active CNV lesions secondary to age-related macular degeneration (AMD);
Subjects must have been responsive to anti-VEGF therapy as assessed by the PI prior to study treatment
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
12 participants in 3 patient groups
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Central trial contact
Youchen Chen
Data sourced from clinicaltrials.gov
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