IP Library › Granted Patent US 11,564,922
Granted Patent B2
US 11,564,922 · App. 17/732,070 · Granted Jan 31, 2023

Methods of treating crohn's disease and ulcerative colitis

Inventors: Aileen L. Pangan (La Grange, IL); Roopal B. Thakkar (Lake Forest, IL); Steven Jungerwirth (Glencoe, IL); Ana Paula Machado De Lacerda (Vernon Hills, IL); Anne M. Robinson (Highland, IN); Mohamed-Eslam F. Mohamed (Gurnee, IL); Ahmed A. Othman (Libertyville, IL); Ben Klünder (Ludwigshafen, DE); Wen Zhou (Cambridge, MA)
Assignee: AbbVie Inc.
A61K31/4985A61K9/0053A61K9/48A61K31/495A61P1/00
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Quick Facts
Patent No.
US 11,564,922
App. No.
17/732,070
Granted
Jan 31, 2023
Kind
B2
Abstract

The present disclosure is directed to methods for treating Crohn's disease, and in particular, to methods for inducing clinical remission and/or endoscopic improvement of Crohn's disease, using a JAK1 inhibitor. In certain embodiments, the patient is administered an induction dose of the JAK1 inhibitor to induce clinical remission and/or endoscopic improvement of the Crohn's disease, followed by administration of at least one maintenance dose of the JAK1 inhibitor thereafter. In other embodiments, the present disclosure is directed to methods for treating ulcerative colitis using a JAK1 inhibitor.

Claims (7)

1. A method of treating Crohn's disease in an adult patient having moderately to severely active Crohn's disease to achieve clinical remission, the method comprising:

(a) orally administering to the patient an induction dose of 45 mg of upadacitinib once daily for 12 weeks; and

(b) orally administering to the patient, after the last induction dose of 45 mg of upadacitinib, a maintenance dose of 15 mg of upadacitinib once daily,

wherein the method achieves clinical remission of the Crohn's disease in the patient.

2. The method of claim 1 , wherein the method achieves induction of clinical remission per Crohn's Disease Activity Index (CDAI) at 12 weeks after the administration of the initial induction dose of 45 mg of upadacitinib.

3. The method of claim 1 , wherein the method achieves maintenance of clinical remission per Crohn's Disease Activity Index (CDAI) at 52 weeks after administration of the initial maintenance dose of 15 mg of upadacitinib.

4. The method of claim 1 , wherein prior to receiving the initial induction dose the adult patient had an inadequate response or intolerance to a previous treatment with an anti-TNF agent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2022
From: ABBVIE DEUTSCHLAND GMBH & CO. KG
To: ABBVIE INC.
Reel/Frame 061556/0848 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 13, 2022
From: KLÜNDER, BEN
To: ABBVIE DEUTSCHLAND GMBH & CO. KG
Reel/Frame 061405/0886 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 19, 2022
From: PANGAN, AILEEN L.; THAKKAR, ROOPAL B.; JUNGERWIRTH, STEVEN; MACHADO DE LACERDA, ANA PAULA; ROBINSON, ANNE M.; MOHAMED, MOHAMED-ESLAM F.; OTHMAN, AHMED A.; ZHOU, WEN
To: ABBVIE INC.
Reel/Frame 061131/0544 →
Continuity (11)
Continuation In Part 17667748 · Feb 9, 2022
Continuation In Part 17115833 · Dec 9, 2020
Continuation 15917013 · Mar 9, 2018
Provisional Application 63285916 · Dec 3, 2021
Provisional Application 63211412 · Jun 16, 2021
Provisional Application 63151429 · Feb 19, 2021
Provisional Application 62593629 · Dec 1, 2017
Provisional Application 62483289 · Apr 7, 2017
Provisional Application 62470565 · Mar 13, 2017
Provisional Application 62469337 · Mar 9, 2017
Related Publication 20220273651A1 · Sep 1, 2022
Cited By (1)
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