A Multicenter International Randomized Double-blind Alendronate-controlled Study to Determine the Efficacy and Safety of AMG 785 in the Treatment of Postmenopausal Women with Osteoporosis
Investigational Medication for Postmenopausal Osteoporosis
Brief description of study.
The purpose of this study is to find out more about AMG 785 in women with postmenopausal osteoporosis (thinning of the bones after menopause). This study will see if AMG 785 prevents fractures of the bone and whether it causes any side effects.
Detailed description of study
The purpose of this study is to find out more about AMG 785 in women with postmenopausal osteoporosis (thinning of the bones after menopause). This study will see if AMG 785 prevents fractures of the bone and whether it causes any side effects.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Osteoporosis
-
Age: 60 years - 90 years
-
Gender: Female
This study investigates an investigational medication for women with postmenopausal osteoporosis, which is a condition where bones become thin and fragile after menopause. The purpose of the study is to see if the investigational medication can prevent bone fractures and to monitor any possible side effects.
Participants in this study will receive either the investigational medication or a placebo, which is an inactive substance that looks like the investigational medication but does not contain any medicine. The study will involve regular monitoring of bone health and assessment of side effects.
- Who can participate: Women aged 50 and above who have gone through menopause and have been diagnosed with osteoporosis are eligible to participate.
- Study details: Participants will be randomly assigned to receive either the investigational medication or a placebo. A placebo is an inactive substance that looks like the investigational medication but does not contain any medicine.
Interested in the study?
Select a study center that’s convenient for you, and get in touch with the study team.
Please choose between Voice or SMS based delivery of verification code
or