Status:
COMPLETED
A Study Comparing Oral Calcitonin to Nasal Spray Calcitonin in Postmenopausal Osteoporotic Women
Lead Sponsor:
Tarsa Therapeutics, Inc.
Conditions:
Osteoporosis, Postmenopausal
Eligibility:
FEMALE
45+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to compare the effectiveness and tolerability of two medications, calcitonin nasal spray and a tablet containing calcitonin, in postmenopausal women with osteoporosis. Ost...
Detailed Description
This was a randomized, double-blind, double-dummy, multiple dose, placebo-controlled, parallel group, 48- week, Phase III study. Women age 45 and over who were postmenopausal and had a diagnosis of os...
Eligibility Criteria
Inclusion
- Female and age 45 or over.
- Must have undergone the onset of spontaneous or surgical menopause. Spontaneous menopause is defined as 12 months of spontaneous amenorrhea or 6 months of spontaneous amenorrhea with serum Follicle Stimulating Hormone (FSH) levels \>40 milli-international units (mIU)/milliliter (mL) or 6 weeks post-surgical bilateral oophorectomy with or without hysterectomy.
- Diagnosis of osteoporosis on the basis of an axial lumbar spine, femoral neck or total hip BMD which is below the mean for premenopausal women by a magnitude of at least 2.5 SD or 2.0 SD, if there is a documented history of a vertebral fragility fracture.
- Must have at least three contiguous lumbar vertebrae (L1-L4) that are evaluable by DXA for BMD that is, without fracture or significant degenerative disease, as determined by Bio-Imaging Technologies, Inc.
- No clinically significant abnormal findings in the medical history, physical exam or nasal exam.
- No clinically significant abnormal laboratory values at the screening assessment.
Exclusion
- History of severe allergic disease.
- History of metabolic and other bone diseases, including osteogenesis imperfecta, osteomalacia, and Paget's disease.
- Vitamin D insufficiency defined as a 25 hydroxyvitamin D level \<20 ng/mL.
- Use of any intravenous bisphosphonate in the past 24 months, or \>2 doses of intravenous bisphosphonate ever.
- Use of oral bisphosphonate before randomization, including investigational bisphosphonates, unless: 1) less than 6 months of treatment and off for 6 months, or 2) 6 to 12 months of treatment and off for 2 years, or 3) More than 12 months of treatment and off for 5 years
- Use of denosumab, fluoride, or strontium, ever.
- Use of parathyroid hormone analogs or other bone metabolic agents within 1 year preceding randomization.
- Any condition or disease that may interfere with the ability to have a DXA scan or to evaluate a DXA scan, for example, severe osteoarthritis of the spine, spinal fusion, pedicle screws, history of vertebroplasty, or degenerative disease that results in insufficient number of evaluable lumbar vertebrae, or more than 1 lumbar vertebral fracture in L1 through L4. (More than 4 vertebral fractures in T4 through L4; Bilateral hip replacements)
- Use of anabolic steroids or androgens within 6 months preceding randomization.
- Use of Vitamin D metabolites and analogs, (e.g., calcitriol) within 3 months preceding randomization). Note: Vitamin D supplementation is not exclusionary.
- Use of estrogen or estrogen-related drugs, for example, tamoxifen, tibolone, or raloxifene within 3 months preceding randomization.
- Use of coumadin within 4 weeks preceding randomization or heparin within 1 week preceding randomization.
- Chronic systemic treatment with glucocorticoids, hormone replacement therapy, calcitonin or any other medication within the previous three months which, in the opinion of the Investigator, would interfere with the study.
- Clinically relevant abnormal history, physical findings or laboratory values at the pre-study screening assessment that could interfere with the objectives of the study or the safety of the patient.
- Presence of acute or chronic illness or history of chronic illness which, in the judgment of the Investigator, makes participation in the study medically inappropriate.
- Uncontrolled hypertension, significant gastrointestinal abnormalities, uncontrolled diabetes mellitus, significant coronary heart disease, any psychotic mental illness, chronic allergic rhinitis, asthma, uncorrected endocrine dysfunction, or significantly impaired hepatic, respiratory or renal function.
- History of drug or alcohol abuse, or intake of more than 30 units of alcohol weekly.
Key Trial Info
Start Date :
June 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2011
Estimated Enrollment :
565 Patients enrolled
Trial Details
Trial ID
NCT00959764
Start Date
June 1 2009
End Date
February 1 2011
Last Update
November 19 2013
Active Locations (20)
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1
Rheumatology Associates of N. AL, P.C.
Huntsville, Alabama, United States, 35801
2
Northern California Institute for Bone Health, Inc.
Oakland, California, United States, 94609
3
Desert Medical Advances
Palm Desert, California, United States, 92260
4
Bethesda Health Research Center/Bone Health Center of Bethesda
Bethesda, Maryland, United States, 20817