drugset / Trial / NCT01965509
A PK/PD Study of Polyethylene Glycol Loxenatide in Patients With Type 2 Diabetes
Phase 2
Completed
120 enrolled
Jiangsu HengRui Medicine Co., Ltd.
China-Japan Friendship Hospital · 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 the effective therapeutic concentration range of PEX168, also decided to observe safety and PK/PD correlation by long-term continuous administration.
Timeline
- Start
- 2012-05
- Primary completion
- 2013-08
- Completion
- 2013-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PEGLOXENATIDE | Peptide | 100 ug | Subcutaneous |
| Subject | PEGLOXENATIDE | Peptide | 200 ug | Subcutaneous |