IP Library Granted Patent US 9,790,267
Granted Patent B2
US 9,790,267 · App. 14/181,870 · Granted Oct 17, 2017

Glypican-3-specific antibody and uses thereof

Inventor: David Kaplan (Media, PA)
Assignees: The Trustees of the University of Pennsylvania; The United States of America, as represented by the Secretary of the Department of Veterans Affairs
C07K16/18C07K14/70521C07K16/2809C07K16/30C07K16/303G01N33/57438C07K2317/622C07K2317/92
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Quick Facts
Patent No.
US 9,790,267
App. No.
14/181,870
Granted
Oct 17, 2017
Kind
B2
Abstract

The present invention relates to compositions and methods for diagnosing and treating diseases, disorders or conditions associated with dysregulated expression of GPC3. The invention provides novel antibodies that specifically bind to glypican-3 (GPC3). The invention also relates to a fully human chimeric antigen receptor (CAR) wherein the CAR is able to target GPC3.

Claims (4)

1. An isolated and substantially purified polynucleotide encoding a single chain human anti-glypican-3 (GPC3) antibody fragment, wherein the single chain antibody fragment comprises a heavy chain variable region and light chain variable region, wherein the amino acid sequence of the heavy chain variable region and the amino acid sequence of the light chain variable region are selected from the group consisting of: (a) SEQ ID NO: 12 and SEQ ID NO: 17; (b) SEQ ID NO: 13 and SEQ ID NO: 18; (c) SEQ ID NO: 14 and SEQ ID NO: 19; and, (d) SEQ ID NO: 15 and SEQ ID NO: 20.

2. The isolated polynucleotide of claim 1 , comprising nucleic acid sequences that encode the heavy chain variable region and light chain variable region, wherein the heavy chain variable region-encoding nucleic acid sequence and the light chain variable region-encoding nucleic acid sequence are selected from the group consisting of: (a) SEQ ID NO: 52 and SEQ ID NO: 57; (b) SEQ ID NO: 53 and SEQ ID NO: 58; (c) SEQ ID NO: 54 and SEQ ID NO: 59; and, (d) SEQ ID NO: 55 and SEQ ID NO: 60.

3. An isolated and substantially purified vector comprising the isolated polynucleotide of claim 1 .

4. The vector of claim 3 , wherein the vector is a viral vector selected from the group consisting of an adenoviral vector, an adeno-associated virus vector, a retroviral vector, a poxvirus, a herpes simplex virus I, and a lentiviral vector.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 16, 2014
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034012/0374 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2014
From: KAPLAN, DAVID
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA; GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF VETERANS AFFAIRS
Reel/Frame 032780/0838 →
Continuity (3)
Continuation PCTUS2012062765 · Oct 31, 2012
Provisional Application 61557174 · Nov 8, 2011
Related Publication 20140170114A1 · Jun 19, 2014