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Safety and Efficacy of Abaloparatide-SC in Men With Osteoporosis (ATOM)

Osteoporosis Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Phase 3 Multicenter Study to Evaluate the Safety and Efficacy of Abaloparatide-SC for the Treatment of Men With Osteoporosis

Clinical Trial Summary

A 12-month study to measure the efficacy and safety of abaloparatide in men with osteoporosis.

Clinical Trial Description

The primary objective of this prospective controlled study is to evaluate the efficacy and the safety of abaloparatide 80 micrograms (mcg) per day administered subcutaneously (SC) compared to placebo in men with osteoporosis. Efficacy was primarily assessed by the change in bone mineral density (BMD) over 12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03512262
Study type Interventional
Source Radius Health, Inc.
Contact
Status Completed
Phase Phase 3
Start date May 3, 2018
Completion date September 8, 2021
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