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Withdrawn Phase 3 Interventional

A Study to Evaluate Efficacy and Safety of Subcutaneous Abatacept With Steroid Treatment Compared to Steroid Treatment Alone in Adults With Giant Cell Arteritis (GCA)

ClinicalTrials.gov ID: NCT03192969

Public ClinicalTrials.gov record NCT03192969. 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 Jul 22, 2026, 5:49 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 Phase III Randomized, Placebo-Controlled, Double-Blind Clinical Trial to Evaluate the Efficacy and Safety of Subcutaneous Abatacept in Combination With Glucocorticoid Treatment Compared to Glucocorticoid Monotherapy in Adults With Giant Cell Arteritis

Study identification

NCT ID
NCT03192969
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Abatacept Drug
  • Placebo Other
  • Glucocorticoid Treatment Drug

Drug · Other

Eligibility (public fields only)

Age range
50 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
Jul 14, 2017
Primary completion
Jun 6, 2020
Completion
Nov 22, 2021
Last update posted
Jul 11, 2017

2017 – 2021

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Local Institution Phoenix Arizona 85032
Local Institution Fullerton California 92835
Local Institution West Hollywood California 90048
Local Institution Denver Colorado 80230
Local Institution Iowa City Iowa 52242
Local Institution Kansas City Kansas 66160
Local Institution Rochester Minnesota 55905-0001
Local Institution New York New York 10021
Local Institution Cleveland Ohio 44195
Local Institution Dayton Ohio 45417
Local Institution Philadelphia Pennsylvania 19104
Local Institution Charleston South Carolina 29406
Local Institution Beaumont Texas 77702

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 86 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03192969, 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 Jul 11, 2017 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03192969 live on ClinicalTrials.gov.

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