drugset / Trial / NCT00638781

Desmoteplase in Acute Ischemic Stroke (DIAS)

NCT00638781 ↗

Phase 2 Completed 104 enrolled PAION Deutschland GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

The DIAS study (Part 2) was performed to support the dose finding of desmoteplase treatment in subjects with acute ischemic stroke selected by perfusion/diffusion mismatch on MRI within a time window of 3 to 9 h after stroke-symptom onset. In addition, it assessed safety and tolerability of 3 doses of desmoteplase compared with placebo with special consideration of intracranial hemorrhage and major systemic bleedings.

Timeline

Start
2001-03
Primary completion
2003-10
Completion
2003-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Desmoteplase Protein / enzyme biologic 62.5 ug/kg Intravenous
Comparator Desmoteplase Protein / enzyme biologic 90 ug/kg Intravenous
Comparator Desmoteplase Protein / enzyme biologic 125 ug/kg Intravenous

Indications