A Single Center Study to Evaluate the Efficacy and Safety of ETC 1002 in Subjects With Type 2 Diabetes
Completed · Phase 2 · Has a placebo group
Conditions studied: Hyperlipidemia, Type 2 Diabetes
In brief
This Phase 2 study will asses the LDL-C lowering efficacy of ETC-1002 versus placebo in subjects with type 2 diabetes.
Key facts
- Study ID
- NCT01607294
- Run by
- Esperion Therapeutics, Inc.
- People needed
- 60
- Starts
- 2012-04-01
- Expected to finish
- 2012-10-01
- Last updated by the study team
- 2019-03-29
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of type 2 diabetes meeting all of the following:
- Minimum 6 month history of diabetes prior to screening visit;
- Fasting C-peptide ≥ 0.8 ng/mL at screening visit;
- HbA1C at screening visit 7-10%;
- Fasting glucose from 140-270 mg/dL on Day -7 following washout of all glucose regulating drugs and supplements.
- BMI at screening visit from 25-35 kg/m2;
- LDL-C at screening ≥ 100 mg/dL
Where it is running
- Study site — Miramar, Florida, United States
Full record on ClinicalTrials.gov
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