Skip to content

Osteoclast Inhibition and Bone Formation

Effects of Age and Osteoclast Inhibition on Bone Formation

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02554695
Enrollment
81
Registered
2015-09-18
Start date
2015-10-20
Completion date
2016-10-25
Last updated
2018-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Bone Loss

Keywords

adrenergic

Brief summary

This protocol addresses: 1) How gene expression changes in bone cells are affected by aging? 2) Is aging associated with decreased signaling between bone cells? 3) How does treatment with the osteoporosis medication denosumab affect bone cell signaling?

Detailed description

This protocol collectively addresses the following goals: 1) What are the changes in gene expression in osteoblasts and osteocytes that lead to impaired bone formation with aging; 2) Since recent work from the investigators' group has demonstrated that osteoclasts produce a number of growth factors and cytokines (coupling factors) that enhance osteoblast proliferation and/or differentiation, is aging associated with reduced osteoclast coupling factor production; and 3) If osteoclasts are markedly reduced using the FDA-approved medication for osteoporosis, denosumab, how does that effect the quantity of coupling factors in the bone microenvironment and the target genes of these coupling factors in osteoblasts?

Interventions

DRUGplacebo

subcutaneous saline injection

DRUGdenosumab

single subcutaneous injection of denosumab 60 mg

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Inclusion Criteria: * normal premenopausal women aged 25-40 years * normal postmenopausal women aged 60-80 years * at least 5 yrs since their last menses * follicle stimulating hormone (FSH) \> 20 IU/L *

Exclusion criteria

* Abnormality in any of the screening laboratory studies * Presence of significant liver or renal disease * Malignancy (including myeloma) * Malabsorption * Diabetes * Hypoparathyroidism * Hyperparathyroidism * Acromegaly * Cushing's syndrome * Hypopituitarism * Severe chronic obstructive pulmonary disease * Undergoing treatment with any medications that affect bone turnover, including the following: * adrenocorticosteroids (\> 3 months at any time or \> 10 days within the previous yr) * anticonvulsant therapy (within the previous year) * pharmacological doses of thyroid hormone (causing decline of thyroid stimulating hormone below normal) * calcium supplementation of \> 1200 mg/d (within the preceding 3 months) * bisphosphonates (within the past 3 yrs) * denosumab * estrogen (E) therapy within the past year * treatment with a selective E receptor modulator within the past year * teriparatide within the past yr * Clinical history of osteoporotic fracture (vertebral, hip, or distal forearm) * Recent (within the past 6 months) fracture * Serum 25-hydroxyvitamin D levels of \< 20 ng/ml

Design outcomes

Primary

MeasureTime frameDescription
Gene expression changes in bone cells3 monthsRatio of selected genes as expressed between each of the 3 arms (i.e. relative runx2 gene expression levels in each arm).

Secondary

MeasureTime frameDescription
Osteoclast-osteoblast coupling factor changes3 monthsRatio of selected genes as expressed between each of the 3 arms (i.e. relative runx2 gene expression levels in each arm).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026