IP Library Granted Patent US 9,624,295
Granted Patent B2
US 9,624,295 · App. 11/786,459 · Granted Apr 18, 2017

Uses and compositions for treatment of psoriatic arthritis

Inventors: John R. Medich (East Hanover, NJ); Robert L. Wong (Basking Ridge, NJ); Renee J. Perdok (Gurnee, IL); Eric H. Sasso (Evanston, IL); Rebecca S. Hoffman (Wilmette, IL); Phillip Mease (Seattle, WA); Christopher T. Ritchlin (Canandaigua, NY)
Assignee: Abbvie Biotechnology Ltd.
C07K16/241A61K2039/505A61K2039/545A61K2039/55C07K2317/21C07K2317/565C07K2317/76G01N2800/102
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Quick Facts
Patent No.
US 9,624,295
App. No.
11/786,459
Granted
Apr 18, 2017
Kind
B2
Abstract

The invention provides methods, uses and compositions for the treatment of psoriatic arthritis. The invention describes methods and uses for treating psoriatic arthritis, wherein a TNFα inhibitor, such as a human TNFα antibody, or antigen-binding portion thereof, is used to psoriatic arthritis in a subject. Also described are methods for determining the efficacy of a TNFα inhibitor for treatment of psoriatic arthritis in a subject.

Claims (8)

1. A method of treating a subject having oligoarthritis with a tender joint count (TJC)<5 or a swollen joint count (SJC)<5, in association with psoriatic arthritis, the method comprising administering to the subject about 40 mg of adalimumab once subcutaneously every other week,

wherein at least an ACR20 response is achieved following a treatment period of at least about 12 weeks and the at least an ACR20 response is maintained following a treatment period of at least about 48 weeks,

thereby treating the subject having psoriatic arthritis with oligoarthritis in association with psoriatic arthritis.

2. The method of claim 1 , wherein at least an ACR50 response achieved by the subject following a treatment period of about 12 weeks and the at least an ACR50 response is maintained following a treatment period of at least about 48 weeks.

3. The method of claim 1 , wherein said treatment period is about 48 weeks.

4. The method of claim 2 , wherein said treatment period is about 48 weeks.

5. The method of claim 1 , wherein at least an ACR70 response is achieved by the subject following a treatment period of about 12 weeks and the at least an ACR 70 response is maintained following a treatment period of at least about 48 weeks.

6. The method of claim 5 , wherein said treatment period is about 48 weeks.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2017
From: MEASE, PHILIP
To: ABBVIE BIOTECHNOLOGY LTD
Reel/Frame 043150/0853 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2017
From: SASSO, ERIC H.
To: ABBVIE BIOTECHNOLOGY LTD
Reel/Frame 041551/0983 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2016
From: MEDICH, JOHN R.; WONG, ROBERT L.; PERDOK, RENEE J.; HOFFMAN, REBECCA S.; RITCHLIN, CHRISTOPHER T.
To: ABBVIE BIOTECHNOLOGY LTD.
Reel/Frame 038529/0228 →
Continuity (7)
Provisional Application 60790909 · Apr 10, 2006
Provisional Application 60809770 · May 30, 2006
Provisional Application 60815489 · Jun 20, 2006
Provisional Application 60858376 · Nov 10, 2006
Provisional Application 60899262 · Feb 2, 2007
Provisional Application 60909683 · Apr 2, 2007
Related Publication 20090028794A1 · Jan 29, 2009