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Clinical Trials/NCT00557310
NCT00557310
Completed
Phase 4

The Effects of Teriparatide on Bone Microarchitecture as Determined by High Resolution Magnetic Resonance Imaging and Digital Topological Analysis

Eli Lilly and Company1 site in 1 country35 target enrollmentNovember 2007

Overview

Phase
Phase 4
Intervention
teriparatide
Conditions
Osteoporosis, Postmenopausal
Sponsor
Eli Lilly and Company
Enrollment
35
Locations
1
Primary Endpoint
Percent Change From Baseline in Surface-to-Curve Ratio (SCR) in the Distal Radius at Month 18 Endpoint
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to use imaging technologies to demonstrate the effects of teriparatide on bone structure following 18 to 24 months of therapy in postmenopausal women with osteoporosis.

Detailed Description

As teriparatide is approved for up to 24 months of treatment in the US, patients will be given the option to continue in a 6-month extension phase upon completion of 18 months of teriparatide treatment. This extension will allow for collection of additional bone quality data. In Canada, the use of teriparatide is currently approved for 18 months. Patients in Canada may be given the opportunity to participate in the 6-month extension phase, contingent upon Health Canada approval of the use of teriparatide treatment for 24 months.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
May 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • postmenopausal (after the "change of life") women with osteoporosis
  • between the ages of 45-85
  • have low bone mass as determined by a bone density test
  • have at least one prior atraumatic vertebral or nonvertebral fracture(with a T-score of -2.0 or lower at the lumbar spine, total hip, or femoral neck) or, no prior fracture (with a T-score of -3.0 or lower at these same sites)
  • could have taken up to 5 years total of certain oral osteoporosis medications such as alendronate, risedronate, or ibandronate

Exclusion Criteria

  • have conditions that would affect the bone in the region of the wrist or have had a previous fracture of either wrist which might affect results of study
  • have a metal implant or have had a hip replacement in either hip which might affect results of study
  • have an increased risk of osteosarcoma; includes Paget's disease of bone, a previous bone tumor, or x-ray treatment to the skeleton
  • currently have active or suspected diseases that affect the bone, other than osteoporosis
  • have abnormal levels of calcium, parathyroid hormone in blood, or other laboratory values

Arms & Interventions

Teriparatide

20 micrograms (mcg) teriparatide subcutaneous injection per day for 18 months, with possibility to continue for 24 months

Intervention: teriparatide

Outcomes

Primary Outcomes

Percent Change From Baseline in Surface-to-Curve Ratio (SCR) in the Distal Radius at Month 18 Endpoint

Time Frame: Baseline, 18 months

SCR is a measure of the computed ratio of plate-like to rod-like structures in a given volume of trabecular bone and reflects the integrity of the trabecular network. The higher the value for SCR, the more intact the trabecular network. Least squares (LS) mean of the percent change from baseline to 18 months is from a mixed model repeated measurements analysis. The model included terms for investigator site, prior bisphosphonate use, visit and baseline.

Secondary Outcomes

  • Percent Change From Baseline in Volumetric Bone Mineral Density (BMD) of Lumbar Spine at Month 18 Endpoint(Baseline, 18 months)
  • Percent Change From Baseline in Bone Volume (BV)/Total Volume (TV) Ratio in the Distal Radius at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Surface-to-Curve Ratio (SCR) in the Distal Radius at Month 24 Endpoint(Baseline, 24 months)
  • Percent Change From Baseline in Cortical Thickness (CT) in the Distal Radius at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Topological Erosion Index (TEI) in the Distal Radius at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Volumetric Bone Mineral Density (BMD) of Hip at Month 18 Endpoint(Baseline, 18 months)
  • Percent Change From Baseline in the Estimate of Bone Strength of Lumbar Spine at Month 18 Endpoint(Baseline, 18 months)
  • Percent Change From Baseline in the Estimate of Bone Strength of Hip at Month 18 Endpoint(Baseline, 18 months)
  • Percent Change From Baseline in Areal BMD at the Lumbar Spine at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Areal BMD at the Femoral Neck at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Areal BMD Responses at Total Hip at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Serum Procollagen Type I N-Terminal Propeptide (PINP) at Month 3, 6 and 24 Endpoint(Baseline, 3, 6, 24 months)
  • Percent Change From Baseline in Serum Carboxyterminal Cross-Linking Telopeptide of Type I Collagen (CTX) at Month 3, 6 and 24 Endpoint(Baseline, 3, 6, 24 months)
  • Percent Change From Baseline in Surface-to-Curve Ratio (SCR) at Month 3, 6, 12, 18 and 24 Endpoint(Baseline, 3, 6, 12, 18, 24 months)
  • Percent Change From Baseline in Areal BMD at ⅓ Distal Radius at Month 18 and 24 Endpoint(Baseline, 18, 24 months)
  • Percent Change From Baseline in Areal BMD at Ultra-Distal Radius at Month 18 and 24 Endpoint(Baseline, 18, 24 months)

Study Sites (1)

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