Overview
Study In Postmenopausal Women With Type 2 Diabetes Looking At Approved Diabetes Drugs And How They Affect Bone Health
Status:
Completed
Completed
Trial end date:
2010-09-16
2010-09-16
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this study is to determine the effects of rosiglitazone on the bone in postmenopausal women with type 2 diabetes mellitusPhase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
GlaxoSmithKlineTreatments:
Metformin
Rosiglitazone
Criteria
Inclusion Criteria:- Female, >55 to <80 years
- >5 years menopausal
- Type 2 Diabetes Mellitus (T2DM) diagnosis according to American Diabetes Association
(ADA), American Association of Clinical Endocrinologists (AACE), Canadian Diabetes
Association (CDA), World Health Organization/International Diabetes Federation
(WHO/IDF)
- Drug-naïve (HbA1c < or = 9.0%); OR Prior monotherapy, submaximal doses of metformin (<
or = 1000mg Metformin), sulfonylureas (< or = 5mg Glyburide, < or = 10mg Glipizide or
< or = 8mg glimepiride) or full dose Januvia (100mg) (HbA1c < or = 8.5%); OR Prior
monotherapy, > submaximal doses of metformin (>1000mg) or sulfonylureas (>5mg
Glyburide, >10mg Glipizide or >8mg glimepiride) (HbA1c < or = 7.0%)
- Weighs <300 lbs (136.4 kg)
- Two or more vertebra (L1-L4) suitable for BMD measurement by dual x-ray absorptiometry
(DXA)
- Absolute BMD value consistent with T-score >-2.5 at femoral neck, lumbar spine and
total hip
Exclusion Criteria:
- Type 1 Diabetes Mellitus (T1DM) or history of diabetic ketoacidosis (DKA)
- Renal or hepatic disease (clinically significant)
- Hepatocellular reaction, severe edema, or medically serious fluid event associated
with thiazolidinedione (TZD)
- Recent (<6mos) history or clinical intervention for angina or myocardial infarction or
is taking nitrates
- Any stage of heart failure, i.e. New York Heart Association (NYHA) class I-IV
- Systolic BP >160mmHg or diastolic BP >90mmHg while on antihypertensive
- Hypersensitivity to TZDs, biguanides
- Prior treatment with two or more oral anti-diabetic (OAD) agents
- Bilateral hip replacements
- Concurrent diseases affecting bone metabolism
- Active malabsorption syndrome
- Serum calcium outside the central lab reference range
- Thyroid replacement therapy, serum thyroid stimulating hormone (TSH) must be within
range
- Vitamin D deficiency
- Previous treatment with: strontium, intravenous (IV) bisphosphonate, fluoride,
hormones, calcineurin inhibitors or methotrexate
- Chronic systemic corticosteroid [e.g. glucocorticoid, mineralocorticoid] treatment of
no more than two intra-articular injections within the past year or use of oral
parenteral, or long-term, high-dose inhaled corticosteroids