This study is currently not recruiting participants.

An Open-Label Single-Arm Extension Study to Evaluate the Long-Term Safety of Denosumab Administration in Postmenopausal Women with Low Bone Mineral Density

Investigating Long-term Safety of an Investigational Medication in Postmenopausal Women with Low Bone Density

Not Recruiting
18 years - 100 years
Female
Phase N/A
1 Location

Brief description of study.

The purpose of this research study is to evaluate the long-term safety of denosumab in postmenopausal women with low bone mineral density.

Detailed description of study

The purpose of this research study is to evaluate the long-term safety of denosumab in postmenopausal women with low bone mineral density.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Bone Mineral Density
  • Age: 18 years - 100 years
  • Gender: Female

The purpose of this study is to evaluate the long-term safety of an investigational medication in postmenopausal women who have low bone mineral density. Bone mineral density is a measure of the amount of minerals, such as calcium, in a specific volume of bone, which reflects bone strength and health.

Participants in this study will undergo various procedures to monitor their health and the effects of the investigational medication. This may include regular check-ups, bone density scans, and blood tests to ensure safety and gather data on the medication's impact.

  • Who can participate: Postmenopausal women aged 50 and older with low bone mineral density are eligible to participate.
  • Study details: Participants will receive the investigational medication and attend regular health check-ups. A placebo, which is an inactive substance that looks like the investigational medicine but does not contain any medicine, may also be used in the study.
Updated on 19 Feb 2024. Study ID: 1010002391 (0604-31)

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