drugset / Trial / NCT01042964

Safety, Pharmacokinetic and -Dynamic Study of PR-15, an Inhibitor of Platelet Adhesion

NCT01042964 ↗

Phase 1 Completed 30 enrolled AdvanceCor GmbH Procorde GmbH · collab
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

EvaluationDrugModalityDoseRoute
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