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Completed Phase 3 Interventional

Phase III Study of Efficacy and Safety of Secukinumab Versus Placebo, in Combination With Glucocorticoid Taper Regimen, in Patients With Giant Cell Arteritis (GCA)

ClinicalTrials.gov ID: NCT04930094

Public ClinicalTrials.gov record NCT04930094. 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 23, 2026, 1:23 AM 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, Parallel-group, Double-blind, Placebo-controlled, Multicenter Phase III Trial to Investigate the Efficacy and Safety of Secukinumab 300 mg and 150 mg Administered Subcutaneously Versus Placebo, in Combination With a Glucocorticoid Taper Regimen, in Patients With Giant Cell Arteritis (GCA) (GCAptAIN)

Study identification

NCT ID
NCT04930094
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
354 participants

Conditions and interventions

Interventions

  • Secukinumab 300 mg Biological
  • Placebo Other
  • Secukinumab 150 mg Biological

Biological · Other

Eligibility (public fields only)

Age range
50 Years to 100 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 5, 2021
Primary completion
Apr 10, 2025
Completion
Feb 17, 2026
Last update posted
Mar 30, 2026

2021 – 2026

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Cedars Sinai Medical Center Los Angeles California 90048
IRIS Research and Development Plantation Florida 33324
Sarasota Arthritis Res Ctr Sarasota Florida 34239
Novartis Investigative Site Iowa City Iowa 52242
University Of Iowa Iowa City Iowa 52242
Osteoporosis and Clinical Trial Ctr Hagerstown Maryland 21740
Massachusetts General Hospital Boston Massachusetts 02114
West Tennessee Research Institute Jackson Tennessee 38305
Precision Comp Clin Research Grapevine Texas 76051
Advanced Rheumatology of Houston Spring Texas 77382

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 94 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04930094, 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 Mar 30, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04930094 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →