IP Library Granted Patent US 11,242,378
Granted Patent B2
US 11,242,378 · App. 16/896,980 · Granted Feb 8, 2022

Monoclonal antibodies and cocktails for treatment of Ebola infections

Inventors: Zachary A. Bornholdt (Encinitas, CA); Larry Zeitlin (San Diego, CA); Kartik Chandran (Brooklyn, NY); Anna Wec (Lebanon, NH); Laura Walker (Norwich, VT)
Assignees: MAPP BIOPHARMACEUTICAL, INC.; ALBERT EINSTEIN COLLEGE OF MEDICINE; ADIMAB, LLC
C07K16/10A61P31/14A61K39/42A61K2039/505A61K2039/545A61K2039/55A61K2039/57A61K2039/6075A61K2039/62C07K2317/76
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Quick Facts
Patent No.
US 11,242,378
App. No.
16/896,980
Granted
Feb 8, 2022
Kind
B2
Abstract

Described herein are compositions and methods for the prevention and treatment of ebolavirus infection. In certain embodiments of the present invention, monoclonal antibodies substantially, similar to those described herein, as well as affinity matured variants thereof, alone or in combination, provide therapeutic efficacy in a patient against multiple species of ebolavirus.

Claims (12)

1. A composition for the treatment of Ebola, the composition comprising:

a therapeutically effective combination of

i. a first monoclonal antibody or antigen binding fragment thereof comprising a heavy chain variable region comprising an amino acid sequence at least 90% identical to SEQ ID NO: 15, and affinity matured variants thereof; and a light chain variable region comprising an amino acid sequence at least 90% identical to SEQ ID NO: 18, and affinity matured variants thereof, wherein said first monoclonal antibody or antigen binding fragment thereof has a heavy chain CDR1 comprising SEQ ID NO: 41, a heavy chain CDR2 comprising SEQ ID NO: 42, a heavy chain CDR3 comprising SEQ ID NO: 43, a light chain CDR1 comprising SEQ ID NO: 44, a light chain CDR2 comprising SEQ ID NO: 45, and a light chain CDR3 comprising SEQ ID NO: 46, and wherein the antigen to which the antigen binding fragment binds comprises Ebola glycoprotein; and

ii. a pharmaceutically acceptable excipient or carrier.

2. The composition of claim 1 , wherein said first monoclonal antibody or antigen binding fragment thereof binds at least two species of Ebola glycoprotein.

3. The composition of claim 1 , wherein the first monoclonal antibody or antigen binding fragment that binds to the Ebola glycoprotein comprises predominantly a single glycoform.

4. The composition of claim 3 , wherein the predominantly single glycoform is one of GnGn, G1/G2, and NaNa.

5. The composition of claim 3 , wherein the predominantly single glycoform substantially lacks at least one of fucose and xylose.

6. The composition of claim 2 , further comprising a second monoclonal antibody or antigen binding fragment thereof, wherein said second monoclonal antibody or antigen binding fragment thereof binds Ebola glycoprotein.

7. A monoclonal antibody or antigen binding fragment thereof effective to treat Ebola comprising a heavy chain variable region comprising an amino acid sequence at least 90% identical to SEQ ID NO: 15, and affinity matured variants thereof; and a light chain variable region comprising an amino acid sequence at least 90% identical to SEQ ID NO: 18, and affinity matured variants thereof, wherein said monoclonal antibody or antigen binding fragment thereof has a heavy chain CDR1 comprising SEQ ID NO: 41, a heavy chain CDR2 comprising SEQ ID NO: 42, a heavy chain CDR3 comprising SEQ ID NO: 43, a light chain CDR1 comprising SEQ ID NO: 44, a light chain CDR2 comprising SEQ ID NO: 45, and a light chain CDR3 comprising SEQ ID NO: 46, wherein said monoclonal antibody or antigen binding fragment thereof comprises predominantly a single glycoform that binds at least two species of Ebola, and wherein the antigen to which the antigen binding fragment binds comprises Ebola glycoprotein.

8. The monoclonal antibody or antigen binding fragment thereof of claim 7 , wherein the predominantly single glycoform is one of GnGn, G1/G2, and NaNa.

9. The monoclonal antibody or antigen binding fragment thereof of claim 7 , wherein the predominantly single glycoform substantially lacks at least one of fucose and xylose.

Assignments (5)
CONFIRMATORY LICENSE Recorded Aug 2, 2021
From: MAPP PHARMACEUTICAL, INC.
To: DEFENSE THREAT REDUCTION AGENCY, US DOD
Reel/Frame 057052/0447 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2021
From: WALKER, LAURA
To: ADIMAB, LLC
Reel/Frame 055095/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2021
From: BORNHOLDT, ZACHARY A; ZEITLIN, LARRY
To: MAPP BIOPHARMACEUTICAL, INC.
Reel/Frame 055095/0854 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2021
From: CHANDRAN, KARTIK; WEC, ANNA
To: ALBERT EINSTEIN COLLEGE OF MEDICINE, INC.
Reel/Frame 055096/0121 →
MERGER Recorded Feb 1, 2021
From: ALBERT EINSTEIN COLLEGE OF MEDICINE, INC.
To: ALBERT EINSTEIN COLLEGE OF MEDICINE
Reel/Frame 055096/0400 →
Continuity (3)
Continuation 15898524 · Feb 17, 2018
Provisional Application 62460200 · Feb 17, 2017
Related Publication 20200354437A1 · Nov 12, 2020
Cited By (1)
US 12,209,117