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Completed Phase 3 Interventional Results available

Efficacy and Safety of Denosumab Compared With Risedronate in Individuals Taking Glucocorticoids

ClinicalTrials.gov ID: NCT01575873

Public ClinicalTrials.gov record NCT01575873. 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 Sep 2, 2026, 10:08 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, Active-controlled Study to Evaluate the Efficacy and Safety of Denosumab Compared With Risedronate in Glucocorticoid-treated Individuals

Brief summary

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

This is a 2-year study to evaluate the effect of denosumab versus risedronate in adults with glucocorticoid-induced osteoporosis.

Study identification

NCT ID
NCT01575873
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
795 participants

Conditions and interventions

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
Mar 27, 2012
Primary completion
Jun 20, 2016
Completion
Jun 28, 2017
Last update posted
Jul 26, 2018

2012 – 2017

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Research Site Birmingham Alabama 35294
Research Site Sacramento California 95817
Research Site Lakewood Colorado 80227
Research Site Pembroke Pines Florida 33029
Research Site Gainesville Georgia 30501
Research Site Chicago Illinois 60611
Research Site Evanston Illinois 60201
Research Site Indianapolis Indiana 46202
Research Site Bethesda Maryland 20817
Research Site Cumberland Maryland 21502
Research Site Boston Massachusetts 02118
Research Site Detroit Michigan 48236
Research Site Fargo North Dakota 58103
Research Site Fargo North Dakota 58104
Research Site Mayfield Ohio 44143
Research Site Duncansville Pennsylvania 16635
Research Site Wyomissing Pennsylvania 19610
Research Site Beckley West Virginia 25801

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 81 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01575873, 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 26, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01575873 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →