A Multicenter Study to Evaluate the Effects of DR-105 on Bone Mineral Density in Adolescent Females

Status:	Archived
Conditions:	Orthopedic
Therapuetic Areas:	Orthopedics / Podiatry
Healthy:	No
Age Range:	Any
Updated:	7/1/2011
Start Date:	June 2009
End Date:	March 2012

A Multicenter, Open-Label, Randomized, Controlled Study to Compare the Effects on Bone Mineral Density of DR-105 and a 28-Day Cycle Oral Contraceptive Regimen in Healthy, Postmenarchal, Adolescent Females

This study is being conducted to compare the effects of DR-105 to a 28-day oral
contraceptive regimen on bone mineral density (BMD) in adolescent females. Subjects will be
randomized to either DR-105 or a 28-day oral contraceptive (OC). Subjects not seeking
hormonal contraception who meet eligibility criteria will serve as a control group. Duration
of the study for study subjects will be approximately 13 months.

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A Multicenter Study to Evaluate the Effects of DR-105 on Bone Mineral Density in Adolescent Females

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A Multicenter, Open-Label, Randomized, Controlled Study to Compare the Effects on Bone Mineral Density of DR-105 and a 28-Day Cycle Oral Contraceptive Regimen in Healthy, Postmenarchal, Adolescent Females

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