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

2014-08-27 03:18:26 | BioPortfolio

Summary

Primary Objective is to determine the effectiveness of RGN475/SAR164877 in reducing pain associated with vertebral fracture.

Secondary Objective is to determine the overall safety and tolerability of RGN475/SAR164877 in the patients with vertebral fracture pain.

Description

The duration of participation in this study for each patient is approximately 13 weeks

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Back Pain

Intervention

REGN475/SAR164877, Placebo

Location

Sanofi-Aventis Investigational Site Number 840007
Huntsville
Alabama
United States
35801

Status

Recruiting

Source

Sanofi-Aventis

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:18:26-0400

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