IP Library › Granted Patent US 9,663,579
Granted Patent B2
US 9,663,579 · App. 15/215,012 · Granted May 30, 2017

Formulation for anti-α4β7 antibody

Inventors: Irving H. Fox (Wellesley, MA); Catherine Scholz (Woburn, MA)
Assignee: Millennium Pharmaceuticals, Inc.
C07K16/2839A61K39/39591A61K2039/505A61K2039/54A61K2039/545C07K2317/14C07K2317/24C07K2317/565C07K2317/92
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Quick Facts
Patent No.
US 9,663,579
App. No.
15/215,012
Granted
May 30, 2017
Kind
B2
Abstract

Methods for achieving clinical response of Crohn's disease in a human patient are described comprising administration of an antibody that has binding specificity for human α4β7 integrin using a safe dosing regimen of these antibody formulations that is easy to follow, and which results in a therapeutically effective amount of the anti-α4β7 antibody in vivo.

Claims (6)

1. A method for achieving clinical response of Crohn's disease in a human patient, comprising intravenously administering to a human patient with Crohn's disease, wherein said human patient had a lack of an adequate response with, lost response to, or was intolerant to a TNFα antagonist: a first dose of 300 mg of an antibody that has binding specificity for human α4β7 integrin, a second dose of 300 mg of the antibody two weeks after the first dose, and a third dose of 300 mg of the antibody six weeks after the first dose, wherein the antibody comprises the heavy chain variable region sequence of amino acids 20 to 140 of SEQ ID NO:2, and the light chain variable region sequence of amino acids 20 to 131 of SEQ ID NO:4.

2. The method of claim 1 , wherein heavy chain of the antibody comprises amino acids 20 to 470 of SEQ ID NO:2, and the light chain of the antibody comprises amino acids 20 to 238 of SEQ ID NO:4.

3. The method of claim 1 , wherein each dose is intravenously administered as an infusion over about 30 minutes.

4. The method of claim 1 , wherein the Crohn's disease is moderate to severely active Crohn's disease.

5. A method for achieving clinical response of Crohn's disease in a human patient, comprising intravenously administering to a human patient with Crohn's disease, wherein the human patient had a lack of an adequate response with, lost response to, or was intolerant to a TNFα antagonist: a first dose of 300 mg of vedolizumab, a second dose of 300 mg of vedolizumab two weeks after the first dose, and a third dose of 300 mg of vedolizumab six weeks after the first dose.

6. The method of claim 5 , wherein the Crohn's disease is moderate to severely active Crohn's disease.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2023
From: MILLENNIUM PHARMACEUTICALS, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 064700/0474 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2017
From: FOX, IRVING H.; SCHOLZ, CATHERINE
To: MILLENNIUM PHARMACEUTICALS, INC.
Reel/Frame 041398/0933 →
Continuity (5)
Continuation 13462414 · May 2, 2012
Provisional Application 61585859 · Jan 12, 2012
Provisional Application 61550545 · Oct 24, 2011
Provisional Application 61481533 · May 2, 2011
Related Publication 20160340432A1 · Nov 24, 2016