drugset / Trial / NCT01965496
A Phase I Study of Polyethylene Glycol Loxenatide in Patients With Type 2 Diabetes
Phase 1
Completed
64 enrolled
Jiangsu HengRui Medicine Co., Ltd.
People's Liberation Army General Hospital of Chengdu Military Region · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PEGLOXENATIDE | Peptide | 100 ug | Subcutaneous |
| Subject | PEGLOXENATIDE | Peptide | 200 ug | Subcutaneous |
| Subject | PEGLOXENATIDE | Peptide | 300 ug | Subcutaneous |