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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 Oct 18, 2026, 8:22 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, 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 28, 2012 (Actual)
Primary completion
Jun 21, 2016 (Actual)
Completion
Jun 29, 2017 (Actual)
Last update posted
Jul 27, 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 27, 2018 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01575873 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →