Inhibition of neovascularization with a soluble chimeric protein comprising VEGF FLT-1 and KDR domains
View Patent ↗Described herein are novel soluble chimeric fusion proteins comprising amino acid sequences derived from the vascular endothelial growth factor (VEGF) receptors flt-1 and KDR, including domain 4 of KDR. The claimed chimeric fusion proteins antagonize the endothelial cell proliferative and angiogenic activity of VEGF and are useful in the treatment of neovascularization-related disease.
1. A method for treating an angiogenesis-related eye disease or condition, comprising:
administering to a subject in need thereof, either locally or intravenously, a VEGF receptor fusion protein comprising the amino acid sequence of SEQ ID NO:8,
wherein one or more symptoms of the angiogenesis-related eye disease or condition is improved following administration.
2. The method according to claim 1 , wherein the angiogenesis-related eye disease or condition is selected from the group consisting of age-related macular degeneration (AMD), diabetic retinopathy, choroidal neovascularization (CNV), cystoid macular edema, diabetic macular edema, retinal vascular occlusion, corneal neovascularization, corneal transplantation, neovascular glaucoma, pterygium, chronic conjunctivitis, angiogenesis related therapy failure such as laser coagulation, and surgical retinal transplantation.
3. The method according to claim 2 , wherein the angiogenesis-related eye disease or condition is AMD.
4. The method according to claim 2 , wherein the angiogenesis-related eye disease or condition is diabetic retinopathy.
5. The method according to claim 2 , wherein the one or more improved symptoms of the angiogenesis-related eye disease or condition is selected from the group consisting of a decrease in mean choroidal neovascularization (CNV) leakage, improved mean visual acuity, a reduction in mean foveal retinal thickness, a reduction in mean macular size, and a reduction in mean lesion size.
6. The method according to claim 5 , wherein the one or more symptoms of the angiogenesis-related eye disease or condition remains improved for at least 7 months following the administration.
7. The method according to claim 1 , wherein the fusion protein is administered by intravitreal injection.
8. The method according to claim 7 , wherein the fusion protein is administered by an intravitreal injection comprising an amount of from about 0.01 to about 100 mg or from about 0.1 to about 10 mg.
9. The method according to claim 8 , wherein following a single intravitreal injection of the fusion protein, the one or more symptoms of the angiogenesis-related eye disease or condition that is improved is selected from the group consisting of a decrease in mean choroidal neovascularization (CNV) leakage, improved mean visual acuity, a reduction in mean foveal retinal thickness, a reduction in mean macular size, and a reduction in mean lesion size.
10. The method according to claim 9 , wherein the one or more symptoms of the angiogenesis-related eye disease or condition remains improved for at least 7 months following the administration.
11. The method according to claim 1 , wherein the fusion protein is administered by intravenous injection.
12. The method according to claim 11 , wherein the fusion protein is administered by an intravenous injection comprising an amount of of from about 0.1 to about 30 mg/kg or from about 0.5 to about 5 mg.
13. The method according to claim 1 , wherein the fusion protein is administered using eye drops.
14. The method according to claim 13 , wherein the fusion protein is administered by eye drops comprising an amount of from about 0.1 to about 50 mg per eye drop or from about 0.5 to about 5 mg per eye drop.
15. The method according to claim 1 , wherein the fusion protein is provided in a formulation that further comprises one or more pharmaceutically acceptable carriers commonly used for ophthalmological therapeutics.
16. The method according to claim 15 , wherein the fusion protein is provided as a solution formulation.
17. The method according to claim 16 , wherein a 10 mg/ml solution of the fusion protein is stable for at least 24 months at a temperature of −20° C. or for at least 12 months at a temperature of 4° C.
18. The method according to claim 15 , wherein the fusion protein is lyophilized.