drugset / Trial / NCT01965496

A Phase I Study of Polyethylene Glycol Loxenatide in Patients With Type 2 Diabetes

NCT01965496

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Polyethylene Glycol Loxenatide (PEX168) is a new human glucagon-like peptide 1 (GLP-1) analogue that created on the basis of the Exenatide and modified by polyethylene glycol (PEG). This study aims to evaluate whether the titration mode of administration could reduce the incidence of adverse reactions of PEX168, also decided to observe long-term continuous administration of PK/PD correlation.

Timeline

Start
2012-03
Primary completion
2013-03
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject PEGLOXENATIDE Peptide 100 ug Subcutaneous
Subject PEGLOXENATIDE Peptide 200 ug Subcutaneous
Subject PEGLOXENATIDE Peptide 300 ug Subcutaneous