Acute Hip Fracture Study in Patients 65 Years or Greater

Status Completed

Clinical Trial Summary

This is a randomized, double-blind, parallel group, placebo-controlled, multicenter study to investigate the safety, tolerability, and efficacy of VK5211 after 12 weeks of treatment. Males and females ≥65 years old who are ambulatory and recovering from a hip fracture will be eligible for participation 3-7 weeks post-injury.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02578095
Study type	Interventional
Source	Viking Therapeutics, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	October 30, 2015
Completion date	March 2018

View Details

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