Psoriasis Clinical Trial

AMG 827 in Subjects With Psoriatic Arthritis

Summary

The study will examine the safety and effectiveness of AMG 827 for the treatment of psoriatic arthritis

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Full Description

The study will examine the safety and effectiveness of AMG 827 for the treatment of psoriatic arthritis. Patients will randomly receive either AMG 827 or placebo (a look-a-like liquid that does not have any drug in it) and neither the doctor nor the patient will know what treatment is being given.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subject has had a diagnosis of psoriatic arthritis (by the Classification of Psoriatic Arthritis (CASPAR) criteria) for at least 6 months
Subject has ≥ 3 tender and ≥ 3 swollen joints

Exclusion Criteria:

Subject has an active infection or history of infections (systemic anti-infectives were used within 28 days; requiring hospitalization or intravenous anti-infectives within 8 weeks; recurrent or chronic)
Significant concurrent medical conditions
Pregnant or breast feeding
Significant Laboratory abnormalities
Use of sulfasalazine, hydroxychloroquine, systemically administered calcineurin inhibitors, azathioprine, parenteral corticosteroids including intramuscular or intraarticular administration, or live vaccines within 28 days
Use of anti-TNF therapy within 2 months
Use of an anti-interleukin (IL)12/IL-23 drug or other experimental or commercially available biologic therapies for psoriasis and/or psoriatic arthritis within 3 months
Prior use of rituximab
Prior use of anti-IL-17 biologic therapy, including AMG 827

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

168

Study ID:

NCT01516957

Recruitment Status:

Terminated

Sponsor:

Bausch Health Americas, Inc.

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There are 31 Locations for this study

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Research Site
Peoria Arizona, 85381, United States
Research Site
Scottsdale Arizona, 85258, United States
Research Site
Tucson Arizona, 85711, United States
Research Site
Hemet California, 92543, United States
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Huntington Beach California, 92646, United States
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La Jolla California, 92037, United States
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Los Angeles California, 90095, United States
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Palm Desert California, 92260, United States
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Palo Alto California, 94304, United States
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Victorville California, 92395, United States
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Sarasota Florida, 34239, United States
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Boise Idaho, 83702, United States
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Lexington Kentucky, 40504, United States
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Baton Rouge Louisiana, 70809, United States
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Frederick Maryland, 21702, United States
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Grand Rapids Michigan, 49546, United States
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Lansing Michigan, 48910, United States
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Lebanon New Hampshire, 03756, United States
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Rochester New York, 14642, United States
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Portland Oregon, 97239, United States
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Duncansville Pennsylvania, 16635, United States
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Seattle Washington, 98122, United States
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Victoria British Columbia, V8P 5, Canada
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Winnipeg Manitoba, R3A 1, Canada
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St. John's Newfoundland and Labrador, A1A 5, Canada
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St. John's Newfoundland and Labrador, A1C 5, Canada
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Newmarket Ontario, L3Y 3, Canada
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Ottawa Ontario, K1H 8, Canada
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Trois-Rivieres Quebec, G8Z 1, Canada
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QC , G1W 4, Canada
Research Site
Quebec , G1V 3, Canada

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

168

Study ID:

NCT01516957

Recruitment Status:

Terminated

Sponsor:


Bausch Health Americas, Inc.

How clear is this clinincal trial information?

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