IP Library Granted Patent US 12,098,187
Granted Patent B2
US 12,098,187 · App. 16/770,840 · Granted Sep 24, 2024

Bispecific HIV-1-neutralizing antibodies

Inventors: David D. Ho (Chappaqua, NY); Yaoxing Huang (Brooklyn, NY); Jian Yu (New Providence, NJ)
Assignee: The Trustees of Columbia University in the City of New York
C07K16/1063A61K39/42A61P31/18C07K16/2812C07K16/2866A61K2039/505C07K2317/24C07K2317/31C07K2317/52C07K2317/567C07K2317/66C07K2317/76C07K2317/94
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Quick Facts
Patent No.
US 12,098,187
App. No.
16/770,840
Granted
Sep 24, 2024
Kind
B2
Abstract

In various embodiments, the present invention relates generally to using bispecific antibodies in the prevention and treatment of HIV.

Claims (9)

1. A bispecific antibody in a CrossMab format capable of neutralizing HIV, wherein the antibody comprises a light chain and heavy chain portion of a first antibody that binds to a HIV envelope protein, and a light chain and heavy chain portion of a second antibody ibalizumab that binds to a cell membrane receptor protein or a cell membrane co-receptor protein,

wherein the first antibody is selected from the group consisting of:

10E8.2, wherein the light chain portion of 10E8.2 comprises SEQ ID NO: 33, and the heavy chain portion of 10E8.2 comprises SEQ ID NO: 34;

10E8.2.1, wherein the light chain portion of 10E8.2.1 comprises SEQ ID NO: 33, and the heavy chain portion of 10E8.2.1 comprises SEQ ID NO: 35;

10E8.2.2, wherein the light chain portion of 10E8.2.2 comprises SEQ ID NO: 33, and the heavy chain portion of 10E8.2.2 comprises SEQ ID NO: 36;

10E8.2.3, wherein the light chain portion of 10E8.2.3 comprises SEQ ID NO: 33, and the heavy chain portion of 10E8.2.3 comprises SEQ ID NO: 37;

the light chain portion of the second antibody ibalizumab comprises an amino acid sequence identical to SEQ ID NO: 1, and the heavy chain portion of the second antibody ibalizumab comprises an amino acid sequence identical to SEQ ID NO: 2.

2. A pharmaceutical composition comprising the bispecific antibody of claim 1 , and a pharmaceutically acceptable carrier.

3. The pharmaceutical composition of claim 2 , wherein the composition is formulated for oral, intranasal, pulmonary, intradermal, transdermal, subcutaneous, intramuscular, intraperitoneal, or intravenous delivery.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2021
From: HO, DAVID D; HUANG, YAOXING; YU, JIAN
To: AARON DIAMOND AIDS RESEARCH CENTER
Reel/Frame 055812/0896 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2020
From: THE AARON DIAMOND AIDS RESEARCH CENTER FOR THE CITY OF NEW YORK, INC.
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 054339/0333 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2020
From: THE AARON DIAMOND AIDS RESEARCH CENTER FOR THE CITY OF NEW YORK, INC,
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 052961/0266 →
Continuity (5)
Continuation 15850832 · Dec 21, 2017
Continuation In Part 15414822 · Jan 25, 2017
Division 14558341 · Dec 2, 2014
Provisional Application 61910685 · Dec 2, 2013
Related Publication 20210087259A1 · Mar 25, 2021