drugset / Trial / NCT00615966
Phase 2 Study of the Safety of Diannexin in Kidney Transplant Recipients
Phase 2
Completed
58 enrolled
Alavita Pharmaceuticals Inc
CTI Clinical Trial and Consulting Services · collab
RandomizedParallel-groupQuadruple-blindPrevention
Summary
The purpose of this study is evaluate the safety and tolerability of Diannexin in kidney transplant recipients.
Timeline
- Start
- 2008-02
- Primary completion
- 2009-01
- Completion
- 2010-02
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | DIANEXIN | Unknown | 200 ug/kg | Intravenous |
| Subject | DIANEXIN | Unknown | 400 ug/kg | Intravenous |
Indications
No indication recorded.