IP Library Granted Patent US 8,758,748
Granted Patent B2
US 8,758,748 · App. 12/973,155 · Granted Jun 24, 2014

Anti-angiogenic therapy

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Quick Facts
Patent No.
US 8,758,748
App. No.
12/973,155
Granted
Jun 24, 2014
Kind
B2
Abstract

The present invention provides novel monoclonal antibodies directed to PlGF and fragments and derivatives thereof, more particularly to humanized antibodies and fragments thereof for use in the treatment and/or prevention of pathological angiogenesis.

Claims (6)

1. A method for reducing side effects of a VEGF-inhibiting anti-angiogenic agent in a therapy for inhibiting undesired angiogenesis, said method comprising decreasing, in said therapy, the effective amount of said VEGF-inhibiting anti-angiogenic agent and adding a PlGF-neutralizing agent, such combined therapy reducing said side effects, said PlGF-neutralizing agent being an antibody comprising a variable heavy chain sequence of which the sequence of the CDR1, CDR2, and CDR3 region corresponds to the sequence of SEQ ID NO: 17, 18, and 19, respectively, and comprising a variable light chain sequence of which the sequence of the CDR1, CDR2, and CDR3 region corresponds to the sequence of SEQ ID NO: 20, 21, and 22, respectively.

2. A method for inhibiting undesired angiogenesis, said method comprising adding a PlGF-neutralizing agent to a therapy for inhibiting undesired angiogenesis with a VEGF-inhibiting anti-angiogenic agent, wherein the effective amount of the VEGF-inhibiting anti-angiogenic agent in said therapy is decreased compared to its effective amount in a therapy for inhibiting undesired angiogenesis with the VEGF-inhibiting anti-angiogenic agent, such combined therapy inhibiting undesired angiogenesis, said PlGF-neutralizing agent being an antibody comprising a variable heavy chain sequence of which the sequence of the CDR1, CDR2, and CDR3 region corresponds to the sequence of SEQ ID NO: 17, 18, and 19, respectively, and comprising a variable light chain sequence of which the sequence of the CDR1, CDR2, and CDR3 region corresponds to the sequence of SEQ ID NO: 20, 21, and 22, respectively.

3. The method of claim 1 wherein said PlGF-neutralizing agent and said VEGF-inhibiting anti-angiogenic agent are combined via simultaneous or sequential administration.

4. The method of claim 1 wherein said undesired angiogenesis is a pathological condition selected from the group consisting of cancer, inflammation, adhesion formation, diseases of the eye, pulmonary hypertension and vascular leakage.

5. The method of claim 2 wherein said PlGF-neutralizing agent and said VEGF-inhibiting anti-angiogenic agent are combined via simultaneous or sequential administration.

6. The method of claim 2 wherein said undesired angiogenesis is a pathological condition selected from the group consisting of cancer, inflammation, adhesion formation, diseases of the eye, pulmonary hypertension and vascular leakage.

Assignments (5)
CHANGE OF NAME Recorded Feb 13, 2019
From: THROMBOGENICS N.V.
To: OXURION NV
Reel/Frame 049255/0733 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2011
From: COLLEN, DESIRE
To: LIFE SCIENCES RESEARCH PARTNERS VZW
Reel/Frame 025730/0923 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2011
From: STASSEN, JEAN-MARIE
To: THROMB-X N.V.
Reel/Frame 025730/0984 →
MERGER Recorded Feb 2, 2011
From: THROMB-X N.V.
To: THROMBOGENICS N.V.
Reel/Frame 025731/0104 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2011
From: CARMELIET, PETER
To: VLAAMS INTERUNIVERSITAIR INSTITUUT VOOR BIOTECHNOLOGIE VZW
Reel/Frame 025728/0388 →