Overview
A Study to Evaluate the Safety and Efficacy of CCX140-B in Subjects With Type 2 Diabetes Mellitus
Status:
Completed
Completed
Trial end date:
2010-11-01
2010-11-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to evaluate the safety and potential effectiveness of CCX140-B in subjects with Type 2 diabetes mellitus.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
ChemoCentryxTreatments:
Pioglitazone
Criteria
Key Inclusion Criteria:- Diagnosed type 2 diabetes mellitus
- Must have a body mass index ≥25 and <45 kg/m2, but if body mass index is ≥25 and <28
kg/m2, then waist circumference must be >94 cm for men and >80 cm for women
- Must be on a stable dose of metformin for at least 8 weeks prior to randomization
- Hemoglobin A1c (HbA1c) of 6.5 to 10.0% inclusive and fasting plasma glucose 135 to 270
mg/dL inclusive at Screening
Key Exclusion Criteria:
- Type 1 diabetes mellitus or history of diabetic ketoacidosis
- Received insulin treatment within 12 weeks of randomization
- Received chronic (more than 7 days) systemic glucocorticoid treatment within 12 weeks
of randomization
- Received sulfonylurea, thiazolidinedione, exenatide, or any other glucose lowering
treatment (other than metformin) within 8 weeks of randomization
- Symptomatic congestive heart failure requiring prescription medication, clinically
evident peripheral edema, poorly-controlled hypertension (systolic blood pressure >160
or diastolic blood pressure >100), history of unstable angina, myocardial infarction
or stroke within 6 months of randomization, or chronic renal failure
- History or presence of drug-induced myopathy, drug-induced creatine kinase elevation,
or leukopenia (WBC count <3.5 x 10(9)/L)
- History or presence of any form of cancer within the 5 years prior to randomization,
with the exception of excised basal cell or squamous cell carcinoma of the skin, or
cervical carcinoma in situ or breast carcinoma in situ that has been excised or
resected completely and is without evidence of local recurrence or metastasis
- Fasting serum triglyceride >400 mg/dL