Overview

Study In Postmenopausal Women With Type 2 Diabetes Looking At Approved Diabetes Drugs And How They Affect Bone Health

Status:
Completed
Trial end date:
2010-09-16
Target enrollment:
0
Participant gender:
Female
Summary
The purpose of this study is to determine the effects of rosiglitazone on the bone in postmenopausal women with type 2 diabetes mellitus
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
GlaxoSmithKline
Treatments:
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