A Phase II Study Evaluating SB-751689 in Post-Menopausal Women With Osteoporosis.
Status and phase
Conditions
Treatments
Details and patient eligibility
About
This is a 12 month study designed to evaluate the safety and effectiveness of SB-751689 in the treatment of osteoporosis in post-menopausal women, in comparison with 2 active comparators and placebo.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion:
- Informed consent: Subject is willing and able to provide written informed consent.
- Menopausal status: Ambulatory female aged < 80 years at screening and >5 years postmenopausal.
- T-Score: A subject with either no or only one prevalent vertebral fracture is eligible for inclusion if she satisfies one of the following T-score requirements:
If no prevalent vertebral fracture subject must have an absolute BMD value consistent with a T-score of less than or equal to -2.5 and greater than -4.0 at either the femoral neck, total hip, trochanter, or lumbar spine, or If one prevalent vertebral fracture subject must have an absolute BMD value consistent with a T-score of less than or equal to -2.0 and greater than -4.0 at either the femoral neck, total hip, trochanter, or lumbar spine.
- Suitable vertebra: Two or more vertebra in the range of L1 to L4 that are suitable for BMD measurement by DXA.
- Protocol compliance: Subject who, in the opinion of the investigator, is willing and able to comply with the requirements of the protocol.
Exclusion:
- T-Score: Has an absolute BMD value consistent with a T-score less than or equal to -4.0 at either the femoral neck, total hip, trochanter, or lumbar spine.
- Vertebral fractures: Has >1 prevalent vertebral fracture at the screening visit.
- Non-vertebral fractures: Any previous non-vertebral osteoporosis related/fragility fracture after age 40.
- Spine deformity: Significant spine deformity which would preclude DXA/QCT assessments.
- BMI: BMI ≥33kg/m2.
- Bone metabolic diseases: Other than osteoporosis, history or concurrent diseases affecting bone metabolism (e.g., osteomalacia, hyperparathyroidism, hyperthyroidism).
- GI disease: History of major upper gastrointestinal disease
- Malabsorption: Active or history of malabsorption (e.g., history of celiac disease, irritable bowel syndrome or inflammatory bowel disease).
- Liver disease: Past or current history of liver disease or known hepatic or biliary abnormalities, (with the exception of previously documented diagnosis of Gilbert's syndrome).
- Rheumatoid arthritis: Active disease or history of rheumatoid arthritis.
- Nephrolithiasis: History of or active nephrolithiasis (kidney stones).
- Osteosarcoma risk: Subjects at increased risk of osteosarcoma such as those with Paget's disease of bone or any prior external beam or implant radiation therapy involving the skeleton.
- Malignancy: Malignant disease diagnosed within the previous 5 years (except resected basal cell cancer).
- Biological abnormalities: Any clinically relevant biological abnormality found and/or volunteered at screening (other than those related to the disease under investigation) which, in the opinion of the investigator, is clinically significant and would preclude safe participation in this study.
- Surgical and medical conditions: Presence of the following conditions within six months prior to screening: myocardial infarction, coronary bypass surgery, coronary artery angioplasty, unstable angina, cardiac arrhythmia, clinically evident congestive heart failure, or cerebrovascular accident.
- Glomerular filtration rate: Glomerular filtration rate (GFR) <35 mL/min as calculated by the Modification of Diet in Renal Disease (MDRD) equation as follows: GFR (mL/min/1.73 m2) = 186 x (Serum creatinine mg/dL)-1.154 x (Age)-0.203 x (0.742 if female) x (1.210 if African American) (conventional units).
- QT/QTc prolongation: A marked baseline prolongation of QT/QTc interval (e.g., QTc interval ≥450 msec on the Screening ECG).
- Torsades de Pointes: A history of risk factors for Torsades de Pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome).
- Liver chemistries: Liver chemistries [aspartate aminotransferase (AST), alanine aminotransferase (ALT) or total bilirubin] exceeding 2-fold the upper limit of the laboratory-specified reference range, at screening.
- Abnormal serum calcium: Serum calcium (total or albumin-adjusted) outside the central laboratory reference range at the screening visit.
- Abnormal PTH: PTH (intact or whole) outside the normal range.
- Abnormal creatine phosphokinase: Creatine phosphokinase (CPK) outside the normal range.
- Abnormal alkaline phosphatase: Alkaline phosphatase outside of the normal range.
- Thyroid hormone replacement: Subjects receiving thyroid hormone replacement therapy must have a TSH level checked. Subjects will be excluded if TSH levels are <0.1 or >10.0mIU/L. However, subjects will not be excluded if TSH is in the range 0.1-4.5 mIU/L. If TSH is >4.5 and ≤10.0mIU/mL, measure T4 and exclude the subject only if the T4 is outside the normal range.
- Vitamin D deficiency: Vitamin D deficiency (serum 25-hydroxy vitamin D < 20ng/mL, equivalent to 50nmol/L) at screening. Subjects can undergo vitamin D repletion as per local practice and be re-screened once only for vitamin D levels within the 6-week screening period. They will remain excluded if the re-screened value is < 20ng/mL.
- Previous strontium or IV bisphosphonate: Any previous treatment with strontium ranelate or intravenous bisphosphonate.
- Oral bisphosphonates: Any previous treatment with an oral bisphosphonate as follows:
any treatment within the last six months
-
one month cumulative treatment within the last 12 months
-
three months cumulative treatment within the past two years, or
-
two years cumulative treatment within the past five years.
- Fluoride: Treatment with fluoride (dose greater than 10mg/day) within the previous 5 years for osteoporosis.
- Digoxin: Current therapy with digoxin.
- Bone metabolism drugs: Treatment with other drugs affecting bone metabolism within the last six months prior to screening:
Chronic systemic corticosteroid [e.g., glucocorticoid, mineralocorticoid] treatment of no more than 2 intra-articular injections within the past year or use of oral, parenteral, or long-term, high-dose inhaled corticosteroids. Treatment with any topical corticosteroid will not exclude the subject from participating.
Hormones [e.g., estrogens/"natural estrogen preparations"(except for nonsystemic vaginal treatment), 19-norprogestins, SERMs such as raloxifene, anabolic steroids/androgens such as dehydroepiandrosterone (DHEA) or its sulfated form (DHEAS), nandrolone, tibolone, active vitamin D analogs/metabolites such as 1,25-dihydroxy vitamin D (calcitriol) or 1alpha-hydroxyvitamin D3 (1-alpha hydroxycholecalciferol), calcitonin].
Calcineurin inhibitors [e.g., cyclosporine, tacrolimus] or methotrexate.
- Previous anabolic agents: Treatment with PTH, PTH analogues or similar anabolic agent for osteoporosis within the last two years.
- Contraindications: Contraindications to therapy with calcium or vitamin D.
- Pregnancy: Women who are pregnant are not allowed in this study.
- Interfering medications: Vitamin A in excess of 10,000 IU per day, heparin, or lithium, or anticonvulsant medications except benzodiazepines.
- Investigational drug exposure: Administration of any investigational drug within 90 days preceding the first dose of the study drug.
- Substance abuse: History or current evidence of drug or alcohol abuse within the previous 12 months.
- Problems swallowing: Inability to swallow a tablet whole.
The following exclusion criteria do not apply to subjects allocated to the open-label teriparatide group:
- Calcium channel blockers: Current therapy with calcium channel blockers diltiazem and verapamil.
- Oral Azole Antifungals: Current therapy with any oral azole antifungal.
- Immunosuppressants: Current therapy with cyclosporine or oral tacrolimus.
- Ritonavir: Current therapy with ritonavir.
- Quinidine: Current therapy with quinidine.
- Macrolide Antibiotics: Subjects anticipated to require chronic use of macrolide antibiotics.
- Alendronate Contraindications: Contraindications to therapy with alendronate. Additional Exclusion Criteria for Subjects Recruited at QCT Sites
- Hip surgery: History of hip surgery resulting in a metal implant on either the left or right side that would cause an artefact on a QCT scan.
Additional Exclusion Criteria for Teriparatide Subjects
- Teriparatide contraindications: Contraindications to therapy with teriparatide according to locally approved datasheet.
Trial design
Primary purpose
Allocation
Interventional model
Masking
564 participants in 4 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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