Real World Evidence in China: Faricimab Use in Diabetic Macular Edema, Retinal Vein Occlusion, and Neovascular Age-Related Macular Degeneration (The Farseeing Study)

Inclusion Criteria:

1. Have signed the informed consent

2. Female and male Chinese patients, who had been diagnosed with nAMD, DME, or RVO byCFP, OCT, FFA, ICGA, or OCTA

3. ≥50 years old for patients with nAMD, ≥18 years old both for patients with DME andRVO, at the time of signing informed consent (or the first administration offaricimab, whichever occurs first)

4. Patients for whom the decision to receive treatment with faricimab is made prior toand independent from study participation

5. Patients have received at least one faricimab treatment (the first dose) in thestudy eye

Exclusion Criteria:

1. Patients not receiving treatment for nAMD/DME/RVO with faricimab according to thestandard of care and in line with the current summary of product characteristics (SPC) / labeling in China

2. Active ocular inflammation or suspected / active ocular infection in either eye

3. Received any other anti-VEGF treatment after faricimab

4. Received any steroid treatment within 6 months (180 days) before the first faricimabtreatment in the study eye

5. Any participation in any other clinical trials currently

6. Patients could not provide the clinical data (visual acuity and OCT images) within 2weeks (14 days) before receiving the initial faricimab injection