ClinicalTrials.gov record
Terminated Phase 2 Interventional

Single Injection of REGN475/SAR164877 in Treatment of Vertebral Fracture Pain

ClinicalTrials.gov ID: NCT01001715

Public ClinicalTrials.gov record NCT01001715. 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 May 14, 2026, 8:34 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

Randomized, Double-blind, Placebo-controlled Study of the Effect of a Single Injection of SAR164877 (REGN475) on Reduction of Pain From Vertebral Fracture Associated With Osteoporosis

Study identification

NCT ID
NCT01001715
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
41 participants

Conditions and interventions

Conditions

Interventions

  • Placebo (for REGN475/SAR164877) Drug
  • REGN475/SAR164877 Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 80 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 31, 2009
Primary completion
Dec 31, 2010
Completion
Dec 31, 2010
Last update posted
May 26, 2013

2009 – 2011

United States locations

U.S. sites
11
U.S. states
5
U.S. cities
11
Facility City State ZIP Site status
Sanofi-Aventis Investigational Site Number 840005 Beverly Hills California 90211
Sanofi-Aventis Investigational Site Number 840001 Fresno California 93710
Sanofi-Aventis Investigational Site Number 840017 Sacramento California 95817
Sanofi-Aventis Investigational Site Number 840028 San Diego California 92103
Sanofi-Aventis Investigational Site Number 840008 Stockton California 95204
Sanofi-Aventis Investigational Site Number 840013 Boynton Beach Florida 33472
Sanofi-Aventis Investigational Site Number 840047 Clearwater Florida 33755
Sanofi-Aventis Investigational Site Number 840034 Atlanta Georgia 30328
Sanofi-Aventis Investigational Site Number 840026 New York New York 11201
Sanofi-Aventis Investigational Site Number 840044 Fort Worth Texas 76117
Sanofi-Aventis Investigational Site Number 840023 Southlake Texas 76092

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01001715, 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 May 26, 2013 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01001715 live on ClinicalTrials.gov.

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