IP Library › Granted Patent US 10,765,724
Granted Patent B2
US 10,765,724 · App. 15/471,790 · Granted Sep 8, 2020

Method of treating psoriasis with increased interval dosing of anti-IL12/23 antibody

Inventors: Marc Chevrier (Spring House, PA); Kamyar Farahi (Spring House, PA); Newman Yeilding (Spring House, PA)
Assignee: Janssen Biotech, Inc.
A61K38/208A01K67/0271A61K38/20A61K39/00A61K39/3955C07K14/5434C07K16/244A61K35/12A61K2035/122A61K2039/505A61K2039/507A61K2039/545C07K16/24C07K2317/34C07K2317/55
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Quick Facts
Patent No.
US 10,765,724
App. No.
15/471,790
Granted
Sep 8, 2020
Kind
B2
Abstract

A method of treating an IL-12/23-related disease in a patient using an increasing dosing interval, comprises increasing the dosing interval of IL-12/IL-23 antibody to a patient, wherein the antibody is administered initially and after 4 weeks, after 16 weeks and after 28 weeks, and increasing the dosing interval after 28 weeks to an increased interval, e.g., every 16, 20 or 24 weeks.

Claims (9)

1. A method of treating psoriasis in a a patient using an increasing dosing or maintenance interval, comprising administering a pharmaceutical composition comprising an antibody to both IL-12 and IL-23 to the patient, wherein the antibody comprises a heavy chain variable amino acid sequence of SEQ ID NO: 7 and a light chain variable amino acid sequence of SEQ ID NO: 8, in an initial dose, a dose 4 weeks after the initial dose and a dose once every 12 weeks for 24 weeks after administration of the initial dose and increasing the dosing interval 28 weeks after administration of the initial dose to a dosing interval of every 24 weeks after identifying the patient as a responder to the antibody 28 weeks after administration of the initial dose, wherein the dose is 45 mg or 90 mg.

2. The method of claim 1 , wherein the step of identifying the patient as a responder to the antibody comprises measuring and identifying the patient as having a PASI75 or PGA 0 or 1 score.

3. The method of claim 1 , wherein the antibody to IL-12 and IL-23 administered to the patient is ustekinumab.

4. The method of claim 1 , wherein the patient does not show an increased risk of immunogenicity.

5. The method of claim 1 , wherein the patient has a PASI75, PASI90 or PGA 0 or 1 score 28 weeks after initial treatment.

6. The method of claim 1 , wherein the patient has a PASI75, PASI90 or PGA 0 or 1 score 52 weeks after initial treatment.

7. The method of claim 1 , wherein the patient has a PASI75, PASI90 or PGA 0 or 1 score 108, 112 and/or 116 weeks after initial treatment.

8. The method of claim 1 , wherein the antibody comprises the heavy chain variable region amino acid sequence of SEQ ID NO: 7 and the light chain variable region amino acid sequence of SEQ ID NO: 8 and comprises about 0.53 mg L-histidine per ml of the pharmaceutical composition; about 1.37 mg L-histidine monohydrochloride monohydrate per ml of the pharmaceutical composition; about 0.04 mg polysorbate 80 per ml of the pharmaceutical composition; about 76 mg of sucrose per ml of the pharmaceutical composition; and water as a diluent at standard state.

9. A method of treating psoriasis in a patient using an a increasing dosing or maintenance interval, comprising administering a pharmaceutical composition comprising an antibody to both IL-12 and IL-23 to the patient in an initial dose, a dose 4 weeks after the initial dose and a dose once every 12 weeks for 24 weeks after administration of the initial dose and increasing the dosing interval 28 weeks after administration of the initial dose to a dosing interval of every 24 weeks after identifying the patient as a responder to the antibody 28 weeks after administration of the initial dose, wherein the dose is 45 mg or 90 mg, and wherein the antibody comprises the heavy chain CDR amino acid sequences of SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 3; and the light chain CDR amino acid sequences of SEQ ID NO: 4, SEQ ID NO: 5, and SEQ ID NO: 6 and comprises about 0.53 mg L-histidine per ml of the pharmaceutical composition; about 1.37 mg L-histidine monohydrochloride monohydrate per ml of the pharmaceutical composition; about 0.04 mg polysorbate 80 per ml of the pharmaceutical composition; about 76 mg of sucrose per ml of the pharmaceutical composition; and water as a diluent at standard state.

Continuity (2)
Provisional Application 62314697 · Mar 29, 2016
Related Publication 20180036379A1 · Feb 8, 2018