drugset / Trial / NCT00501592

Study of INT-747 in Patients With Diabetes and Presumed NAFLD

NCT00501592

Phase 2 Completed 64 enrolled Intercept Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Comparator Obeticholic Acid Small molecule 25 mg Oral
Comparator Obeticholic Acid Small molecule 50 mg Oral