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Terminated Phase 2 Interventional Results available

AMG 827 in Subjects With Psoriatic Arthritis

ClinicalTrials.gov ID: NCT01516957

Public ClinicalTrials.gov record NCT01516957. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 3:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blinded, Placebo-controlled, Multiple-dose Study With an Open Label Extension to Evaluate the Safety and Efficacy of AMG 827 in Subjects With Psoriatic Arthritis.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT01516957
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
168 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2011 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Sep 2015 (Actual)
Last update posted
Aug 27, 2020

2011 – 2015

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Research Site Peoria Arizona 85381 —
Research Site Scottsdale Arizona 85258 —
Research Site Tucson Arizona 85711 —
Research Site Hemet California 92543 —
Research Site Huntington Beach California 92646 —
Research Site La Jolla California 92037 —
Research Site Los Angeles California 90095 —
Research Site Palm Desert California 92260 —
Research Site Palo Alto California 94304 —
Research Site Victorville California 92395 —
Research Site Sarasota Florida 34239 —
Research Site Boise Idaho 83702 —
Research Site Lexington Kentucky 40504 —
Research Site Baton Rouge Louisiana 70809 —
Research Site Frederick Maryland 21702 —
Research Site Grand Rapids Michigan 49546 —
Research Site Lansing Michigan 48910 —
Research Site Lebanon New Hampshire 03756 —
Research Site Rochester New York 14642 —
Research Site Portland Oregon 97239 —
Research Site Duncansville Pennsylvania 16635 —
Research Site Seattle Washington 98122 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01516957, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 27, 2020 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01516957 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →