Enhancing Osteoporosis Therapy: Can We Open the Anabolic Window?

Osteoporosis Clinical Trial

Official title:

Enhancing Osteoporosis Therapy: Can We Open the Anabolic Window?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01166958
• Other study ID #: H-2010-0064
• Status: Completed
• Phase: Phase 4
• First received: July 15, 2010
• Last updated: September 18, 2014
• Start date: September 2010
• Est. completion date: November 2012

Study information

• Verified date: September 2014
• Source: University of Wisconsin, Madison
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Current osteoporosis therapies produce a prompt increase in bone mass, followed by only modest or no further subsequent gains. This limitation, known as the "remodeling transient," reflects the "coupling" of bone resorption with formation such that interventions impacting either of these processes lead to compensatory changes of the other. For example, medications which increase bone formation promptly also stimulate bone resorption. Thus, given the need to dramatically increase bone mass in patients with osteoporosis, it is necessary to "uncouple" formation and resorption. The investigators believe this to be possible using currently existing FDA-approved therapeutic agents, by using a novel, sequential approach.

This pilot project will obtain preliminary data essential to support future work. In this study, the investigators will begin to explore the use of sequential anabolic treatment with teriparatide followed by antiresorptive therapy with raloxifene. The investigators propose that such sequential treatment will allow opening of the "anabolic window," the brief period of time following initiation of teriparatide therapy in which bone formation exceeds resorption.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: November 2012
• Est. primary completion date: November 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 60 Years to 89 Years

Eligibility

Inclusion Criteria:

• Generally healthy, community-dwelling ambulatory post-menopausal women.

• Able and willing to sign informed consent.

• Age 60 to 89.

• Have osteoporosis defined as follows:

• BMD T-score of the lumbar spine, femur neck, total proximal femur or .3 radius of -2.5 to -4.0; note: the lumbar spine must include two vertebrae that are evaluable by DXA in the opinion of the investigator.

OR

• BMD T-score of the lumbar spine, femur neck, total proximal femur or .3 radius of -1.5 or lower and either an atraumatic (in the opinion of the investigator) nonvertebral fracture; [note: nonvertebral fracture sites include the wrist, hip, pelvis, ribs, humerus, clavicle, femur, tibia and fibula] or a minimum of two mild or one moderate or severe atraumatic vertebral fractures (defined using the Genant visual semi-quantitative scale).

• Baseline serum 25(OH)D concentration > 20 ng/ml and < 60 ng/ml.

• Able and willing to receive daily subcutaneous injections using a Forteo® pen.

Exclusion Criteria:

• History of exposure to external beam or implant radiation therapy involving the skeleton.

• Paget's disease or unexplained elevations of alkaline phosphatase.

• Any history of venous thrombosis including deep vein thrombosis, pulmonary embolism, retinal vein thrombosis and superficial phlebitis.

• Documented atherosclerotic vascular disease, including but not limited to prior myocardial infarction, angina, atrial fibrillation, stroke and TIA.

• Marked hypertriglyceridemia (>500 mg/dl).

• History of prior treatment with estrogen resulting in hypertriglyceridemia (> 500 mg/dl).

• Serum calcium, alkaline phosphatase, PTH or TSH outside the normal reference range.

• History of nephrolithiasis or urolithiasis within 10 years prior to enrollment; those with a history of nephro- or urolithiasis must have an appropriate radiology study (e.g., IVP or KUB) within six months documenting absence of stones.

• Baseline 24-hour urine calcium > 250 mg.

• Known risk factors for hypercalcemia, e.g., malignancy, tuberculosis, sarcoidosis.

• History of any form of cancer except adequately treated squamous cell or basal cell skin carcinoma.

• Use of active vitamin D analogs or high dose vitamin D (=50,000 IU weekly) in the last year.

• Active or suspected diseases (within 1 year prior to enrollment) that affect bone metabolism, e.g., renal osteodystrophy, hyperthyroidism, osteomalacia, hyperparathyroidism.

• Known allergy, hypersensitivity, contraindication or intolerance to teriparatide or raloxifene.

• History of vaginal bleeding within the past year.

• Renal failure or substantial hepatic impairment. Note "renal failure" is defined as a calculated creatinine clearance (using the Cockroft-Gault formula) of = 35 ml/minute.

• Severe disease, e.g., cardiac, hepatic, pulmonary, etc., which may limit ability to complete this study. Specifically, significantly impaired hepatic function (ALT or GGT 3x the upper limit of normal.

• Known malabsorption syndromes, e.g., celiac disease, active inflammatory bowel disease, gastric bypass, etc.

• Use of anion exchange resins (e.g., cholestyramine) in the past month.

• Current use of warfarin (coumadin).

• Current use of highly protein-bound drugs including diazepam, diazoxide and lidocaine.

• Current use of digoxin.

• Any prior use of bisphosphonates, denosumab, strontium, fluoride, teriparatide or parathyroid hormone.

• Prior use of estrogen, raloxifene, calcitonin or testosterone will be allowed if discontinued more than six months previously. Low dose intra-vaginal estrogens (0.3 mg or less of conjugated equine estrogen or equivalent) may be continued throughout the study.

• Treatment with glucocorticoids in doses = 5 mg prednisone daily for > 30 days in the prior year.

• Treatment with other drugs known to affect bone metabolism, e.g., anticonvulsants except benzodiazepines or gabapentin, within the prior year. Note: oral calcium supplementation, vitamin D supplementation or diuretic use that has been stable for six months are allowed).

• Treatment within the last 30 days with any drug that has not received regulatory approval.

• Metal in spine precluding spine QCT.

• Any condition that may interfere with evaluation of at least two lumbar vertebrae determined on VFA performed at time of screening. Examples include confluent aortic calcification, severe osteoarthritis, spinal fusion and lumbar spine fractures.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Osteoporosis

Intervention

Drug:
• Teriparatide
Teriparatide (TPD; Forteo) is supplied as a pre-filled syringe that dispenses 20 ug. The dose is one subcutaneous injection daily. Each pre-filled injection delivery device contains sufficient TPD for a 28-day supply of 20 mcg/day.
• Raloxifene
Raloxifene (RLX; Evista) is supplied as a 60 mg tablet. RLX is stored at room temperature.

Locations

Country	Name	City	State
United States	University of Wisconsin Osteoporosis Clinical Center and Research Program	Madison	Wisconsin

Sponsors (1)

Lead Sponsor	Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Serum Markers of Skeletal Turnover (Serum CTX)	Serum CTX was measured at all study visits following the screening visit. The outcome data is an overall average and range from all time points.	These were measured at the baseline and 1, 1.5, 2, 2.5, 3, 4, 5 and 6 month visits.	No
Primary	Serum Markers of Skeletal Turnover (Serum P1NP)	Serum P1NP was measured at all study visits following the screening visit. The outcome data is an overall average and range from all time points.	These were measured at the baseline and 1, 1.5, 2, 2.5, 3, 4, 5 and 6 month visits.	No
Secondary	Average Bone Mineral Density of the Spine at Baseline, 3 Months and 6 Months	Spine BMD was measured at the baseline, three month and six month visits. The outcome data is an overall average and range from all time points.	BMD measured at the baseline, 3 month, and 6 month visits.	No
Secondary	Average Bone Mineral Density of the Proximal Femur (Hip) at Baseline, 3 Months and 6 Months	Hip BMD was measured at the baseline, three month and six month visits. The outcome data is an overall average and range from all time points.	BMD measured at the baseline, 3 month, and 6 month visits.	No
Secondary	Average Bone Mineral Density of the One-third Radius at Baseline, 3 Months and 6 Months	One-third radius BMD was measured at the baseline, three month and six month visits. The outcome data is an overall average and range from all time points.	BMD measured at the baseline, 3 month, and 6 month visits.	No