Safety and Efficacy Study of PN2034 in Type 2 Diabetes Patients on Concomitant Rosiglitazone and Metformin (or Avandamet)

Completed · Phase 2

Conditions studied: Type 2 Diabetes Mellitus

In brief

This study is designed to evaluate the safety and efficacy of PN2034 administered to type 2 diabetics on concomitant rosiglitazone and metformin (or Avandamet) therapy as measured by change in glycosylated hemoglobin (HbA1c) levels from baseline to Week 12. Also the study will evaluate the effect of PN2034 on glucose control as measured by fasting plasma glucose (FPG) and on fasting lipid levels: triglycerides, total cholesterol, high-density lipoproteins (HDL), low-density lipoproteins (LDL), and very low-density lipoproteins (VLDL).

Key facts

Study ID

NCT00110851

Run by

Wellstat Therapeutics

People needed

90

Starts

2005-04-01

Expected to finish

2007-08-01

Last updated by the study team

2007-08-23

Who can join

Age: 21 and older, up to 72. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• diagnosed with type 2 diabetes mellitus
• 21 to 72 years of age
• taking rosiglitazone and metformin (or Avandamet) for at least 3 months, and on a stable dose of rosiglitazone (or Avandamet) for at least 2 months
• glycosylated hemoglobin (HbA1c) level of >/=7.5% but </=10.0%
• fasting blood sugar level >/= 125 mg/dL but </= 279 mg/dL
• BMI 26-43 kg/m2
• direct bilirubin < 1.5x the upper limit of normal (ULN)
• serum creatinine < 1.5 mg/dL (males) or < 1.4 mg/dL (females)
• blood urea nitrogen (BUN)</=40 mg/dL
• all other clinical laboratory parameters (hematology, serum chemistry, and urinalysis) within normal limits or not clinically significant
• ECG normal, or abnormalities not clinically significant
• surgically sterile, postmenopausal, or using adequate contraception and have a negative pregnancy test at Screening
• willing and able to sign an informed consent form

You may not qualify if…

• diagnosed with type 1 diabetes mellitus or has a history of ketoacidosis
• treatment with insulin, TZDs (excluding rosiglitazone) or any other oral or injected antidiabetic (excluding metformin or Avandamet) within 3 months prior to screening or during study treatment
• change in lipid-lowering medication within 2 months of screening
• taken systemic corticosteroids within 1 month prior to screening or during study treatment
• history of or current/active cardiovascular disease
• significant current pulmonary conditions
• significant thyroid disease
• CPK value > 3x ULN
• a female who is pregnant or lactating
• systolic BP > 160 mm Hg or a diastolic BP > 90 mm Hg at screening
• previous or current history of cancer, other than basal cell or stage 1 squamous cell carcinoma of the skin, that has not been in remission within 5 years prior to randomization
• liver function tests (ALT, AST, ALP) > 2 times ULN, or active liver disease at screening
• history of positive HIV
• positive hepatitis B test at screening
• weight loss or gain >/= 15 lbs within 3 months of screening
• history of substance abuse (including alcohol abuse) within 2 years prior to screening
• donated and/or received any blood or blood products within 3 months prior to randomization
• taken an investigational study medication within 30 days prior to screening or during the study

Where it is running

• Phoenix Internal Medicine Associates — Waterbury, Connecticut, United States
• University Clinical Research-DeLand — DeLand, Florida, United States
• Center for Diabetes and Endocrine Care — Hollywood, Florida, United States
• Genesis Research International — Longwood, Florida, United States
• Baptist Diabetes Associates — Miami, Florida, United States
• Andres Patron, DO PA — Pembroke Pines, Florida, United States
• CLIRECO, Inc. — Tamarac, Florida, United States
• Endocrine Clinical Research — Winter Park, Florida, United States
• PRN of Kansas — Wichita, Kansas, United States
• Medical Research Associates of Charlotte — Charlotte, North Carolina, United States
• Neem Research Group of Charlotte — Charlotte, North Carolina, United States
• Unifour Medical Research Associates — Hickory, North Carolina, United States
• Neem Research Group of Raleigh — Raleigh, North Carolina, United States
• Piedmont Medical Research Associates — Winston-Salem, North Carolina, United States
• COR Clinical Research, LLC — Oklahoma City, Oklahoma, United States
• Clinical Research Institute of Southern Oregon, PC — Medford, Oregon, United States
• Camp Hill Clinical Research Center — Camp Hill, Pennsylvania, United States
• Neem Research Group — Columbia, South Carolina, United States
• Palmetto Medical Research Associates — Mt. Pleasant, South Carolina, United States
• Oaks Medical Center — Spring, Texas, United States

Full record on ClinicalTrials.gov

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