IP Library Granted Patent US 8,071,104
Granted Patent B2
US 8,071,104 · App. 12/977,937 · Granted Dec 6, 2011

Neovascular-targeted immunoconjugates

Assignee: Yale University
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Quick Facts
Patent No.
US 8,071,104
App. No.
12/977,937
Granted
Dec 6, 2011
Kind
B2
Abstract

Immunoconjugates for treating diseases associated with neovascularization such as cancer, rheumatoid arthritis, the exudative form of macular degeneration, and atherosclerosis are described. The immunoconjugates typically consist of the Fc region of a human IgG1 immunoglobulin including the hinge, or other effector domain or domains that can elicit, when administered to a patient, a cytolytic immune response or cytotoxic effect against a targeted cell. The effector domain is conjugated to a targeting domain which comprises a factor VII mutant that binds with high affinity and specificity to tissue factor but does not initiate blood clotting such as factor VII having a substitution of alanine for lysine-341 or of alanine for serine-344.

Claims (21)

1. A method for eliciting a cytolytic response to neovasculature associated with an angiogenic disease, wherein the method comprises:

administering to a patient bearing the neovasculature an effective amount of a immunoconjugate protein comprising a human IgG1 immunoglobulin Fc domain conjugated to a mutant form of human factor VII comprising the amino acid sequence encoded by the nucleotide sequence at positions 202-1419 of SEQ ID NO: 12, whereby the neovasculature is destroyed.

2. The method of claim 1 wherein the angiogenic disease is wet macular degeneration.

3. The method of claim 1 wherein the angiogenic disease is cancer.

4. The method of claim 1 wherein the angiogenic disease is an inflammatory disorder.

5. The method of claim 1 wherein the step of administering is intravenous.

6. The method of claim 2 wherein the administering is intraocular.

7. The method of claim 3 wherein the step of administering is via intratumoral injection.

8. The method of claim 1 wherein the step of administering is local.

9. A method for eliciting a cytolytic response to tumor cells expressing tissue factor, wherein the method comprises:

administering to a patient bearing the tumor cells an effective amount of a immunoconjugate protein comprising a human IgG1 immunoglobulin Fc domain conjugated to a mutant form of human factor VII comprising the amino acid sequence encoded by the nucleotide sequence at positions 202-1419 of SEQ ID NO: 12, whereby the tumor cells are cytolytically destroyed.

10. The method of claim 8 wherein the tumor cells are metastatic.

11. A method for eliciting a cytolytic response to pathologic neovasculature associated with a disease, wherein the method comprises:

administering to a patient bearing the neovasculature an effective amount of a immunoconjugate protein comprising a human IgG1 immunoglobulin Fc domain conjugated to a mutant form of human factor VII comprising the amino acid sequence encoded by the nucleotide sequence at positions 202-1419 of SEQ ID NO: 12, whereby the pathological neovasculature is destroyed.

12. The method of claim 11 wherein the disease is wet macular degeneration.

13. The method of claim 11 wherein the disease is cancer.

14. The method of claim 11 wherein the disease is an inflammatory disorder.

15. The method of claim 11 wherein the step of administering is intravenous.

16. The method of claim 12 wherein the administering is intraocular.

17. The method of claim 13 wherein the step of administering is via intratumoral injection.

18. The method of claim 11 wherein the step of administering is local.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2013
From: HU, ZHIWEI
To: YALE UNIVERSITY
Reel/Frame 031727/0261 →
CONFIRMATORY LICENSE Recorded Jan 11, 2011
From: YALE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025615/0674 →
Continuity (5)
Division 11925007 · Oct 26, 2007
Continuation 11134428 · May 23, 2005
Division 10030203
Provisional Application 60142161 · Jul 1, 1999
Related Publication 20110117114A1 · May 19, 2011