CR9112792, a Follow-up of Study CR9108963

CompletedOBSERVATIONAL
Enrollment

171

Participants

Timeline

Start Date

March 31, 2009

Primary Completion Date

June 30, 2009

Study Completion Date

June 30, 2009

Conditions
Osteoporosis
Interventions
PROCEDURE

DXA

CR9112792 is a follow-up study of CR9108963, in which the effects of ronacaleret (100mg, 200mg, 300mg, 400mg) on bone mineral density (BMD), safety and tolerability were evaluated in comparison with placebo and 2 active comparators, alendronate and teriparatide. In this study we will follow-up subjects between 6 and 12 months after they discontinued treatment with placebo or ronacaleret (200mg, 300mg, 400mg) to evaluate the potential for mineralization of bone following cessation of ronacaleret therapy, evaluating lumbar spine and hip BMD by DXA. There is no administration of drug in this study.

Trial Locations (3)

2317

GSK Investigational Site, Hamar

2750

GSK Investigational Site, Ballerup Municipality

5094

GSK Investigational Site, Bergen

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT00891553 - CR9112792, a Follow-up of Study CR9108963 | Biotech Hunter | Biotech Hunter