Claims for Patent: 9,943,573

Summary for Patent: 9,943,573

Title:	Treatment of ocular neovascularization using anti-VEGF proteins
Abstract:	The present disclosure provides compositions and methods for the prevention or treatment of ocular neovascularization, such as AMD, in a human subject, by administering subretinally a pharmaceutical composition comprising a pharmaceutically effective amount of a vector comprising a nucleic acid encoding soluble Fms-related tyrosine kinase-1 (sFlt-1) protein to the human subject.
Inventor(s):	Constable; Ian J. (Mosman Park, AU), Rakoczy; P. Elizabeth (Scarborough, AU), Lai; Chooi-May (Waterford, AU), Chalberg, Jr.; Thomas W. (Redwood City, CA)
Assignee:	Avalanche Australia PTY Ltd. (Southbank Victoria, AU)
Application Number:	14/281,749
Patent Claims:	1. A method for the treatment of ocular neovascularization in a human subject having ocular neovascularization, the method comprising: administering to an eye of the human subject a single dose of a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a recombinant virus comprising a nucleic acid sequence encoding an anti-Vascular Endothelial Growth Factor (VEGF) protein, wherein the single dose comprises at least 1 .times.10.sup.10 and at most 1.times.10.sup.13 vector genomes of the recombinant virus and is sufficient to reduce the ocular neovascularization in the subject for at least one year after the administration of the pharmaceutical composition, wherein between about 5 to 10 days prior to the administration of the pharmaceutical composition a first intravitreal injection of an anti-VEGF agent is administered into the eye of the subject in an amount such that at the time of the administration of the pharmaceutical composition the anti-VEGF agent is present in the eye of the subject at a concentration sufficient to prevent progression of the ocular neovascularization, wherein the subject does not require rescue treatment with an anti-VEGF agent to arrest or reverse progression of the ocular neovascularization at any time after about 90 days and for at least one year following the administration of the pharmaceutical composition, and wherein the nucleic acid sequence comprises in the following order: a) a first ITR sequence; b) a promoter sequence; c) an intron sequence; d) a first UTR sequence; e) the sequence encoding the anti-VEGF protein; f) a second UTR sequence; g) a poly A sequence; and h) a second ITR sequence, wherein the promoter sequence and the sequence encoding the anti-VEGF protein are separated by a sequence that is 300 base pairs or more. 2. The method according to claim 1, wherein the anti-VEGF protein is aflibercept. 3. The method according to claim 1, wherein the anti-VEGF protein comprises a functional fragment of human sFLT1 having a sequence identity of 90% or more to SEQ ID NO:109. 4. The method according to claim 1, wherein the recombinant virus is AAV. 5. The method of claim 1, further comprising performing Fluorescein Angiography (FA) after the administering of the pharmaceutical composition, wherein a reduction in neovascularization is observed by FA. 6. The method of claim 1, further comprising measuring visual acuity by Early Treatment Diabetic Retinopathy Study (ETDRS) letters after the administering of the pharmaceutical composition, wherein the best corrected visual acuity (BCVA) of the human subject decreases by fewer than 15 ETDRS letters following the administering of the pharmaceutical composition. 7. The method of claim 1, further comprising measuring visual acuity by Early Treatment Diabetic Retinopathy Study (ETDRS) letters after the administering of the pharmaceutical composition, wherein the best corrected visual acuity (BCVA) of the human subject improves by at least 1 line as measured by ETDRS letters following the administering of the pharmaceutical composition. 8. The method according to claim 1, wherein the administering comprises subretinal injection. 9. The method according to claim 8, wherein the subretinal injection is within the central retina. 10. The method according to claim 8, further comprising removal of the vitreous gel prior to administering the pharmaceutical composition. 11. The method according to claim 1, wherein said administering comprises injecting the pharmaceutical composition over a period of less than 1 minute. 12. The method according to claim 1, wherein said administering comprises injecting the pharmaceutical composition over a period of 1-3 minutes. 13. The method according to claim 1, wherein said administering comprises injecting the pharmaceutical composition at a rate of about 35 .mu.l/min to about 65 .mu.l/min. 14. The method according to claim 1, wherein said administering comprises injecting the pharmaceutical composition at a rate of about 65 .mu.l/min to about 150 .mu.l/min. 15. The method of claim 1, wherein the intravitreally injected anti-VEGF agent is an anti-VEGF protein. 16. The method of claim 15, wherein the intravitreally injected anti-VEGF protein is ranibizumab. 17. The method of claim 16, wherein a second intravitreal injection of ranibizumab is administered into the eye of the subject within about 30 days of the administration of the pharmaceutical composition.

Details for Patent 9,943,573

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	LUCENTIS	ranibizumab	Injection	125156	06/30/2006		2032-05-15
Genentech, Inc.	LUCENTIS	ranibizumab	Injection	125156	08/10/2012		2032-05-15
Genentech, Inc.	LUCENTIS	ranibizumab	Injection	125156	10/13/2016		2032-05-15
Genentech, Inc.	LUCENTIS	ranibizumab	Injection	125156	03/20/2018		2032-05-15
Regeneron Pharmaceuticals, Inc.	EYLEA	aflibercept	Injection	125387	11/18/2011		2032-05-15
Regeneron Pharmaceuticals, Inc.	EYLEA	aflibercept	Injection	125387	08/16/2018		2032-05-15