drugset / Trial / NCT01042964
Safety, Pharmacokinetic and -Dynamic Study of PR-15, an Inhibitor of Platelet Adhesion
RandomizedSingle-groupOpen-labelTreatment
Summary
Primary objective: To evaluate safety and tolerability, adverse events (AEs), vital signs, ECG, bleeding time, evaluation of antibody titer and safety laboratory tests Secondary objectives: To evaluate the pharmacokinetics and pharmacodynamics (platelet aggregation)of six ascending single intravenous doses of PR-15 in healthy volunteers
Timeline
- Start
- 2006-03
- Primary completion
- 2007-01
- Completion
- 2007-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Revacept | Protein / enzyme biologic | 10 mg | Intravenous |
| Subject | Revacept | Protein / enzyme biologic | 20 mg | Intravenous |
| Subject | Revacept | Protein / enzyme biologic | 40 mg | Intravenous |
| Subject | Revacept | Protein / enzyme biologic | 80 mg | Intravenous |
| Subject | Revacept | Protein / enzyme biologic | 160 mg | Intravenous |