Claims for Patent: 7,306,799

Summary for Patent: 7,306,799

Title:	Use of VEGF inhibitors for treatment of eye disorders
Abstract:	Modified chimeric polypeptides with improved pharmacokinetics and improved tissue penetration are disclosed useful for treating eye disorders, including age-related macular degeneration and diabetic retinopathy.
Inventor(s):	Wiegand; Stanley J. (Croton on Hudson, NY), Papadopoulos; Nicholas J. (LaGrangeville, NY), Yancopoulos; George D. (Yorktown Heights, NY), Fandl; James P. (LaGrangeville, NY), Daly; Thomas J. (New City, NY)
Assignee:	Regeneron Pharmaceuticals, Inc. (Tarrytown, NY)
Application Number:	11/089,803
Patent Claims:	1. A therapeutic method for treating or ameliorating an eye disorder, comprising administering a fusion polypeptide capable of binding vascular endothelial growth factor (VEGF) to a patient in need thereof, wherein the fusion polypeptide consists of an immunoglobulin-like (Ig) domain 2 of a first VEGF receptor Flt1 and Ig domain 3 of a second VEGF receptor Flk1 or Flt4; and a multimerizing component, wherein the multimerizing component is an immunoglobulin domain or fragment of an immunoglobulin domain, wherein the eye disorder is selected from the group consisting of age related macular degeneration and diabetic retinopathy, and wherein administration is selected from the group consisting of eye drops, subconjunctival injection, subconjunctival implant, intravitreal injection, intravitreal implant, sub-Tenon's injection, and sub-Tenon's implant. 2. The therapeutic method of claim 1, wherein the fusion polypeptide comprises SEQ ID NO:6. 3. A therapeutic method for treating or ameliorating an eye disorder, comprising administering a dimeric protein comprising two fusion polypeptides, wherein each fusion polypeptide consists of the amino acid sequence of SEQ ID NO:6, wherein the eye disorder is selected from the group consisting of age related macular degeneration and diabetic retinopathy, and wherein administration is selected from the group consisting of eye drops, subconjunctival injection, subconjunctival implant, intravitreal injection, intravitreal implant, sub-Tenon's injection, and sub-Tenon's implant. 4. A method for the treatment of a human subject diagnosed with age-related macular degeneration, comprising administering an effective amount of a vascular endothelial growth factor (VEGF) inhibitor to the human subject, the method comprising: (a) administering to the subject an initial dose of at least approximately 25-4000 micrograms VEGF inhibitor protein per eye; and (b) administering to the subject a plurality of subsequent doses of the VEGF inhibitor protein in an amount that is approximately the same or less than the initial dose, wherein the subsequent doses are separated in time from each other by at least two weeks, wherein the VEGF inhibitor is a dimeric protein comprising two fusion polypeptides, wherein each fusion polypeptide consists of an immunoglobulin-like (Ig) domain 2 of a first VEGF receptor Flt1 and Ig domain 3 of a second VEGF receptor Flk1 or Flt4, and a multimerizing component, and wherein the multimerizing component is an immunoglobulin domain or fragment of an immunoglobulin domain, and wherein administration is selected from the group consiting of eye drops, subconjunctival injection, subconjunctival implant, intravitreal injection, intravitreal implant, sub-Tenon's injection, and sub-Tenon's implant. 5. The method of claim 4, wherein the initial dose is at least approximately 50 micrograms of VEGF inhibitor protein. 6. The method of claim 5, wherein the initial dose is at least approximately 100 micrograms of VEGF inhibitor protein. 7. The method of claim 6, wherein the initial dose is at least approximately 1000 micrograms of VEGF inhibitor protein. 8. The method of claim 4, wherein the subsequent doses are separated in time from each other by at least four weeks. 9. The method of claim 8, wherein the subsequent doses are separated in time from each other by at least 3 to 6 months. 10. The method of claim 4, wherein the initial dose and at least one subsequent dose is administered by intravitreal injection. 11. The method of claim 4, wherein the VEGF inhibitor is a dimer having two fusion polypeptides, wherein each fusion polypeptide comprises the amino acid sequence of SEQ ID NO:6.

Details for Patent 7,306,799

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Regeneron Pharmaceuticals, Inc.	EYLEA	aflibercept	Injection	125387	11/18/2011		2039-03-29
Regeneron Pharmaceuticals, Inc.	EYLEA	aflibercept	Injection	125387	08/16/2018		2039-03-29

International Patent Family for US Patent 7,306,799

Country	Patent Number	Estimated Expiration
South Africa	200600157
South Africa	200110068
Yugoslavia	86901