DRUG
Romosozumab
romosozumab 210 milligrams monthly
Status
Recruiting
Phase
Phase 4
Enrollment
50
Locations
1
Results
Not posted
Publications
0
Study summary
In this research study the study investigators want to learn more about the effect of two different FDA-approved medication regimens in the treatment of postmenopausal osteoporosis.
Interventions
DRUG
romosozumab 210 milligrams monthly
DRUG
teriparatide 20 micrograms daily
Timeline
First posted
Aug 16, 2024
Study start
Feb 3, 2025
Primary completion
Dec 30, 2027
Study completion
Apr 1, 2028
Results posted
Not reported
Registry updated
Apr 17, 2026
Outcomes
Lumbar spine areal bone mineral density
Time frame · Month 0 to 12
Change in lumbar spine bone density between month 0 and month 12
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * women aged 45+ * postmenopausal * osteoporotic with high risk of fracture Exclusion Criteria: * no significant previous use of bone health modifying treatments * known congenital or acquired bone disease other than osteoporosis * significant renal disease, liver disease, cardiopulmonary disease, or psychiatric disease * abnormal calcium or parathyroid hormone level * serum vitamin D \<20 ng/dL * anemia (hematocrit \<32%) * history of malignancy (except non-melanoma skin carcinoma) * excessive alcohol use or substance abuse * known contraindications to romosozumab or teriparatide
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Massachusetts General Hospital
Boston, Massachusetts, United States
Publications
No PMID-linked publications were present in this registry snapshot.
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Related PeptideStat pages
Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.