Study S000783

A Double-Blind, Multicenter, Randomized Study Evaluating the Safety, Tolerability and Pharmacokinetic/Pharmacodynamic Relationship in T2DMs Treated With 8 Weeks Injection of Polyethylene Glycol Loxenatide

ClinicalTrials.gov record

Registration

Registration: NCT01976858
Study type: INTERVENTIONAL
Allocation: RANDOMIZED
Phase: PHASE1
Masking: QUADRUPLE
Status: COMPLETED
Enrollment: 50
Start: 2011-06
Primary completion: 2011-09
Lead sponsor: Jiangsu HengRui Medicine Co., Ltd.
Conditions: Type 2 Diabetes
Interventions: DRUG:PEX168
Results posted: FALSE

Registered primary outcomes

To determine serum concentrations of PEX168 [8 weeks]

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