IP Library › Granted Patent US 9,809,651
Granted Patent B2
US 9,809,651 · App. 15/047,062 · Granted Nov 7, 2017

Method of treating cancer with an EGFR targeted immunomodulatory fusion protein

Inventors: Nagaraj Govindappa (Karnataka, IN); Kedarnath Sastry (Karnataka, IN); Maria Melina Soares (Karnatake, IN)
Assignee: BIOCON LIMITED
C07K16/2818A61K38/10A61K38/179A61K39/39558A61K45/06C07K7/08C07K14/00C07K14/495C07K14/65C07K14/70532C07K14/70596C07K14/71C07K16/2863C07K16/2866C07K16/2878C07K16/2887C07K16/30C07K16/32G01N33/6854A61K38/00A61K2039/505C07K2317/14C07K2317/24C07K2317/31C07K2317/51C07K2317/515C07K2317/732C07K2319/00C07K2319/02C07K2319/33
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Quick Facts
Patent No.
US 9,809,651
App. No.
15/047,062
Granted
Nov 7, 2017
Kind
B2
Abstract

The present invention relates generally to the field of generating fusion proteins to be used in cancer therapy, and more specifically, to nucleotide sequences encoding the fusion proteins, wherein the chimeric fusion proteins comprises at least one targeting moiety and at least one immunomodulatory moiety that counteracts the immune tolerance of cancer cells.

Claims (6)

1. A method of treating cancer by reducing proliferation of cancer cells, the method comprising contacting cancer cells with a therapeutic amount of chimeric fusion protein, wherein the chimeric fusion protein comprises a targeting moiety to target a cancer cell and an immunomodulating moiety that counteracts immune tolerance, wherein the targeting moiety and the immunomodulating moiety are linked by an amino acid spacer of sufficient length of amino acid residues so that both moieties can successfully bind to their individual targets, wherein the immunomodulating moiety is TGFβRII comprising SEQ ID NO: 4, wherein the amino acid spacer is selected from SEQ ID NO: 3 or SEQ ID NO: 11; and wherein the targeting moiety consists of a light chain of an Anti-EGFR1 antibody; wherein SEQ ID NO: 4 is attached via the amino acid spacer to the C-terminus of the light chain SEQ ID NO: 6 of the Anti-EGFR1 antibody.

2. The method of claim 1 , further comprising administering the chimeric fusion protein in combination with another existing cancer treatment.

3. The method of claim 1 , wherein the amount of TGF-β in a cancerous tumor of the subject is reduced.

4. The method of claim 1 , wherein suppression of an immune system of the subject in the cancer cell is reduced.

5. The method of claim 1 , wherein cytotoxic lymphocytes and Natural Killer cells are activated in the subject.

6. The method of claim 1 , wherein lysis of cancer cells is increased.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2024
From: GOVINDAPPA, NAGARAJ; SASTRY, KEDARNATH; SOARES, MARIA MELINA
To: BIOCON LIMITED
Reel/Frame 067766/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2019
From: GOVINDAPPA, NAGARAJ; SASTRY, KEDARNATH; SOARES, MARIA MELINA
To: BIOCON LIMITED
Reel/Frame 049470/0575 →
Priority Claims (2)
IN 1689/CHE/2012 · Apr 30, 2012 · national
IN 1690/CHE/2012 · Apr 30, 2012 · national
Continuity (3)
Continuation 14458674 · Aug 13, 2014
Division 13779409 · Mar 13, 2013
Related Publication 20160168260A1 · Jun 16, 2016