Regeneron Pharmaceuticals, Inc.

Cincinnati Children's Hospital Medical Center

Regeneran Pharmaceuticals, Inc.

Ivan Borisovich Lobov

Andrew J Murphy

Jesper Gromada

Jee Hwan Kim

Panayiotis Stevis

Yonaton Ray

Stanley J Wiegand

Jingtai Cao

Daniel B Dix

Kenneth S Graham

Karen W Chu

Robert L Vitti

Saurabh Wadhwa

Kristine A Erickson

Richard Lang

Eunice Cheung

The present invention provides apelin receptor (APLNR) modulators that bind to APLNR and methods of using the same. The invention includes APLNR modulators such as antibodies, or antigen-binding fragments thereof, which inhibit or attenuate APLNR-mediated signaling. The invention includes APLNR modulators such as antibodies, or antibody fusion proteins thereof, that activate APLNR-mediated signaling. According to certain embodiments of the invention, the antibodies or antigen-binding fragments or antibody fusion proteins are fully human antibodies that bind to human APLNR with high affinity. The APLNR modulators of the invention are useful for the treatment of diseases and disorders associated with APLNR signaling and/or APLNR cellular expression, such as cardiovascular diseases, angiogenesis diseases, metabolic diseases and fibrotic diseases.

Method of treatment with a fusion protein comprising apelin and an anti-APLNR antibody

The present disclosure provides methods for treating, preventing or reducing the severity of an eye disease. The methods of the present disclosure comprise administering to a subject in need thereof a therapeutic composition comprising an APLNR antagonist such as an anti-APLNR antibody in combination with a vascular endothelial growth factor (VEGF) antagonist (for example, aflibercept).

Methods of treating eye disorders with APLNR antagonists and VEGF inhibitors

The present invention provides methods for treating, preventing or reducing the severity of an eye disease. The methods of the present invention comprise administering to a subject in need thereof a therapeutic composition comprising an angiopoietin-2 (Ang-2) inhibitor such as an anti-Ang-2 antibody in combination with a vascular endothelial growth factor (VEGF) antagonist (e.g., aflibercept).

Methods and formulations for treating vascular eye diseases using aflibercept and nesvacumab

Fusion protein comprising apelin and an anti-APLNR antibody

The present invention provides apelin receptor (APLNR) modulators that bind to APLNR and methods of using the same. The invention includes APLNR modulators such as antibodies, or antigen-binding fragments thereof, that inhibit or attenuate APLNR-mediated signaling. The invention includes APLNR modulators such as antibodies, or antibody fusion proteins thereof, that activate APLNR-mediated signaling. According to certain embodiments of the invention, the antibodies or antigen-binding fragments or antibody fusion proteins are fully human antibodies that bind to human APLNR with high affinity. The APLNR modulators of the invention are useful for the treatment of diseases and disorders associated with APLNR signaling and/or APLNR cellular expression, such as cardiovascular diseases, angiogenesis diseases, metabolic diseases and fibrotic diseases.

Method for treating pathological angiogenesis by administering an antibody that inhibits APLNR

Methods for improving cardiac function by administering an antibody that activates APLNR

APLNR modulators and uses thereof

The present invention provides antibodies that bind to platelet derived growth factor receptor beta (PDGFR-beta) and methods of using the same. According to certain embodiments of the invention, the antibodies are fully human antibodies that bind to human PDGFR-beta with high affinity. The antibodies of the invention are useful for the treatment of diseases and disorders associated with PDGFR-beta signaling and/or PDGFR-beta cellular expression, such as ocular diseases, fibrotic diseases, vascular diseases and cancer.

Anti-PDGFR-beta antibodies and uses thereof

Antibody modulators of APLNR

A method for evaluating in vivo a test substance for angiogenesis modulation activity, including the steps of providing a rodent pup having a pupillary membrane system in a first eye, injecting transcorneally proximate to the pupillary membrane a test substance; and examining the pupillary membrane to determine whether new vascular tissue has grown. The method can also evaluate the ability of a test substance to regress existing vascular tissue, or to inhibit or prevent new vascular tissue, by injecting transcorneally a first substance that induces new vascular tissue growth, then injecting a test substance, and examining the pupillary membrane to determine whether new vascular tissue has grown. The assay can also be used to evaluate the effect of a small molecule on a property of a capillary vessel, and to evaluate a test substance on a problematic vascular condition.

In vivo angiogenesis assay

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New York, NY, United States of America

Ivan Borisovich Lobov