CPC A61K 38/179 (2013.01) [A61K 47/12 (2013.01); A61K 47/183 (2013.01); A61K 47/26 (2013.01); A61K 47/6811 (2017.08); A61P 27/02 (2018.01)] | 17 Claims |
1. A method for treating an angiogenic eye disorder in a human patient, said method comprising a first treatment phase comprising sequentially administering to the patient a VEGF antagonist at 4-week intervals on Day 1, Week 4 and Week 8; wherein the VEGF antagonist comprises amino acid sequence of SEQ ID NO:1, further comprising a second treatment phase, the second treatment phase comprises administering to the patient the VEGF antagonist at 8-week intervals or 12-week intervals until about 36 weeks from the initiation of the treatment, and comprising a third treatment phase, wherein the third treatment phase starts from week 40 and comprises administering the VEGF antagonist on a PRN basis; wherein upon treatment the patient has a decrease in retinal thickness by at least about 80 μm.
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