Safety and Tolerability Study of MBX-2044 in Patients With Type 2 Diabetes

Completed · Phase 2 · Has a placebo group

Conditions studied: Type 2 Diabetes Mellitus

In brief

The purpose of this study is to collect important information regarding the glucose-lowering efficacy of MBX-2044 and the safety of MBX-2044 (especially weight gain and edema) in diabetics. It will also provide important information about the appropriate doses to be used in subsequent longer-term studies to evaluate the safety and efficacy of MBX-2044 alone and in combination with other anti-diabetic agents.

Key facts

Study ID

NCT00422487

Run by

Gilead Sciences

People needed

60

Starts

2006-10-01

Expected to finish

2007-09-01

Last updated by the study team

2015-05-01

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Type 2 diabetes previously controlled with up to one or two non-TZD hypoglycemic agents including sulfonylureas (e.g., glyburide, glipizide, glimeprimide), meglitinides (e.g., Prandin®, Starlix®), metformin (e.g., Glucophage®), α-glucosidase inhibitors (e.g.,acarbose, miglitol) or Byetta®
• All female patients must be either surgically sterile or post-menopausal.
• Male patients with female partners of childbearing potential must agree to use condoms, or their partner must use a medically acceptable form of contraception.
• BMI 24-44 kg/m2.
• Patients must have a FPG ≤ 200 mg/dL at screening.
• Patients must have Hemoglobin A1c ≥ 6.5%, ≤ 10.0% at screening.
• Electrocardiogram (ECG) and chest x-ray must be normal, or considered not clinically significant, for participation in this study.
• Patients must have a blood pressure ≤ 160/90 mm/hg including hypertensive patients controlled with medication.

You may not qualify if…

• History of Type 1 diabetes or diabetes secondary to pancreatitis or pancreatectomy.
• History of TZD use (Actos or Avandia) within 6 months of Screening Visit.
• History of TZD discontinuation due to lack of efficacy.
• History of congestive heart failure within last 5 years.
• History of significant pulmonary disease, myocardial infarction, cerebrovascular accident, or nephrotic syndrome within last 1 year.
• Malignancy within the last 5 years (except resected basal cell carcinoma).
• Ongoing active infection.
• Change in treatment with lipid-lowering agent within 7 days of screening visit.
• Current or expected requirement for anticoagulant therapy [except for low-dose aspirin ≤ 325 mg/d or Plavix® ≤ 75 mg/d].
• Current or expected treatment with phenytoin for the duration of the study.
• Known hypersensitivity to NSAIDs.

Where it is running

• Diabetes and Glandular Disease Research Associates — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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