IP Library › Granted Patent US 11,607,411
Granted Patent B2
US 11,607,411 · App. 17/712,008 · Granted Mar 21, 2023

Methods of treating Crohn's disease and ulcerative colitis

Inventors: Ana Paula Machado De Lacerda (Vernon Hills, IL); Jose Jeffrey V. Enejosa (Chicago, IL); Aileen L. Pangan (La Grange, IL); 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 11,607,411
App. No.
17/712,008
Granted
Mar 21, 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 ulcerative colitis in an adult patient having moderately to severely active ulcerative colitis to achieve clinical remission, the method comprising:

(a) orally administering to the patient an induction dose of 45 mg of upadacitinib once daily for 8 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 ulcerative colitis in the patient.

2. The method of claim 1 , wherein the method achieves induction of clinical remission per Adapted Mayo Score at 8 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 Adapted Mayo Score 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 Dec 16, 2022
From: MACHADO DE LACERDA, ANA PAULA; ENEJOSA, JOSE JEFFREY V.; PANGAN, AILEEN L.; MOHAMED, MOHAMED-ESLAM F.; OTHMAN, AHMED A.; ZHOU, WEN
To: ABBVIE INC.
Reel/Frame 062119/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2022
From: KLÜNDER, BEN
To: ABBVIE DEUTSCHLAND GMBH & CO. KG
Reel/Frame 062119/0827 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2022
From: ABBVIE DEUTSCHLAND GMBH & CO. KG
To: ABBVIE INC.
Reel/Frame 062119/0860 →
Continuity (11)
Continuation 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 20220233527A1 · Jul 28, 2022
Cited By (1)
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