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Completed Phase 3 Interventional Results available

Study of Efficacy and Safety of Brodalumab in Subjects With Psoriatic Arthritis

ClinicalTrials.gov ID: NCT02024646

Public ClinicalTrials.gov record NCT02024646. 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 Apr 29, 2026, 12:44 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-blind, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of Brodalumab in Subjects With Psoriatic Arthritis: AMVISION-2

Study identification

NCT ID
NCT02024646
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
484 participants

Conditions and interventions

Interventions

  • 140 mg brodalumab Drug
  • 210 mg brodalumab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 28, 2014
Primary completion
Sep 30, 2015
Completion
Sep 30, 2015
Last update posted
Aug 19, 2020

2014 – 2015

United States locations

U.S. sites
31
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Research Site Peoria Arizona 85381
Research Site Little Rock Arkansas 72205
Research Site Cypress California 90630
Research Site Hemet California 92543
Research Site Huntington Beach California 92646
Research Site La Jolla California 92037
Research Site Palm Desert California 92260
Research Site Palo Alto California 94304
Research Site Victorville California 92395
Research Site Sarasota Florida 34239
Research Site St. Petersburg Florida 33705
Research Site Tampa Florida 33612
Research Site Tampa Florida 33614
Research Site Chicago Illinois 60611
Research Site Paducah Kentucky 42003
Research Site Baton Rouge Louisiana 70809
Research Site Wheaton Maryland 20902
Research Site Boston Massachusetts 02111
Research Site Battle Creek Michigan 49017
Research Site Grand Rapids Michigan 49546
Research Site Lansing Michigan 48910
Research Site St Louis Missouri 63141
Research Site Las Vegas Nevada 89102
Research Site Rochester New York 14642
Research Site Oklahoma City Oklahoma 73103
Research Site Tulsa Oklahoma 74104
Research Site Dallas Texas 75231
Research Site Dallas Texas 75246
Research Site Waco Texas 76708
Research Site Chesapeake Virginia 23320
Research Site Seattle Washington 98104

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 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02024646, 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 19, 2020 · Synced Apr 29, 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 protocol, eligibility criteria, and contact information for NCT02024646 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →