drugset / Trial / NCT00501592
Study of INT-747 in Patients With Diabetes and Presumed NAFLD
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objectives of this study are to assess, in patients with Type 2 diabetes mellitus (DM) and presumed nonalcoholic fatty liver disease (NAFLD), the following: * The safety and tolerability of multiple doses of INT 747; * The effects of 2 dose levels (25 mg and 50 mg) of INT 747 on insulin resistance and glucose homeostasis; * Effects of INT-747 on hepatocellular function as measured by assessment of liver enzymes and biochemical markers of hepatic and metabolic function and inflammation, and; * Trough concentrations of INT-747 and its metabolites, glyco 6-ethyl chenodeoxycholic acid (6-EDCA) and tauro 6-ECDCA.
Timeline
- Start
- 2007-07
- Primary completion
- 2009-02
- Completion
- 2009-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Obeticholic Acid | Small molecule | 25 mg | Oral |
| Comparator | Obeticholic Acid | Small molecule | 50 mg | Oral |