IP Library Granted Patent US 11,236,158
Granted Patent B2
US 11,236,158 · App. 16/831,351 · Granted Feb 1, 2022

Methods, compositions and dosing regimens for treating or preventing interferon-gamma related indications

Inventors: Cristina De Min (Basel, CH); Walter Ferlin (Basel, CH); Fabrizio De Benedetti (Basel, CH)
Assignee: Swedish Orphan Biovitrum AG
C07K16/249A61K9/0019A61K9/08A61K39/3955A61K45/06A61K47/02A61K47/22A61K47/26A61P7/00A61P29/00A61P37/00A61P37/06A61K2039/505A61K2039/54A61K2039/545C07K2317/21C07K2317/56C07K2317/565C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,236,158
App. No.
16/831,351
Granted
Feb 1, 2022
Kind
B2
Abstract

The disclosure relates generally to methods compositions and dosing regimens for treating, preventing and/or delaying the onset or progression of, or alleviating a symptom associated with elevated IFN-γ levels.

Claims (13)

1. A method of diagnosing and treating graft failure in a patient who has received an allogeneic hematopoietic stem cell transplant comprising:

a. detecting if Chemokine (C-X-C motif) Ligand 9 (CXCL9) is present in a blood sample obtained from the patient;

b. diagnosing the patient with graft failure when CXCL9 is elevated in comparison to a control sample; and

c. administering a Interferon Gamma (IFNγ) antagonist to the patient.

2. The method of claim 1 , wherein CXCL9 is detected by contacting the sample with an anti-CXCL9 antibody and detecting binding between CXCL9 and the anti-CXCL9 antibody.

3. The method of claim 1 , wherein the IFNγ antagonist is an anti-IFNγ antibody.

4. The method of claim 3 , wherein the anti-IFNγ antibody is NI-0501.

5. The method of claim 3 , wherein the anti-IFNγ antibody comprises:

a heavy chain comprising

a variable heavy chain complementarity determining region 1 (VH CDR1) comprising the amino acid sequence of SYAMS (SEQ ID NO: 1); a variable heavy chain complementarity determining region 2 (VH CDR2) comprising the amino acid sequence of AISGSGGSTYYADSVKG (SEQ ID NO: 2); and a variable heavy chain complementarity determining region 3 (VH CDR3) comprising the amino acid sequence of DGSSGWYVPHWFDP (SEQ ID NO: 3); and

a light chain comprising

a variable light chain complementarity determining region 1 (VL CDR1) comprising the amino acid sequence of TRSSGSIASNYVQ (SEQ ID NO: 4); a variable light chain complementarity determining region 2 (VL CDR2) region comprising the amino acid sequence of EDNQRPS (SEQ ID NO: 5); and a variable light chain complementarity determining region 3 (VL CDR3) region comprising the amino acid sequence of QSYDGSNRWM (SEQ ID NO: 6).

6. The method of claim 3 , wherein the anti-IFNγ antibody comprises the heavy chain variable amino acid sequence to the amino acid sequence of SEQ ID NO: 47, and the light chain variable amino acid sequence to the amino acid sequence of SEQ ID NO: 48.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2020
From: DE MIN, CRISTINA; FERLIN, WALTER; DE BENEDETTI, FABRIZIO
To: NOVIMMUNE SA
Reel/Frame 053593/0927 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2020
From: NOVIMMUNE SA
To: EMACO SA
Reel/Frame 053593/0986 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2020
From: EMACO SA
To: SWEDISH ORPHAN BIOVITRUM AG
Reel/Frame 054157/0075 →
Continuity (7)
Division 15792702 · Oct 24, 2017
Continuation In Part 15149633 · May 9, 2016
Provisional Application 62411783 · Oct 24, 2016
Provisional Application 62158153 · May 7, 2015
Provisional Application 62221393 · Sep 21, 2015
Provisional Application 62246949 · Oct 27, 2015
Related Publication 20200291110A1 · Sep 17, 2020
Cited By (2)
US 12,195,530 US 12,297,264