drugset / Trial / NCT02250222

Safety and Tolerability Study of Oral LGD-6972 for Type 2 Diabetes Mellitus

NCT02250222 ↗

Phase 1 Completed 48 enrolled Ligand Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Ligand Pharmaceuticals Incorporated is developing LGD-6972, a novel, orally-bioavailable addition to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. The mechanism of action of LGD-6972 is to reduce the excess liver glucose production characteristic of type 2 diabetes mellitus that is a major contributor to hyperglycemia. This clinical trial will evaluate the safety and tolerability of escalating doses LGD-6972 administered daily over 2 weeks in both healthy subjects and subjects with type 2 diabetes mellitus.

Timeline

Start
2014-10
Primary completion
2015-05
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject LGD-6972 Small molecule 5 mg Oral
Subject LGD-6972 Small molecule 10 mg Oral
Subject LGD-6972 Small molecule 15 mg Oral