Traitements2programmes
Essais1liés
Publications0liées
SourceDBlocale

Traitements

2
MoléculeIndication / populationPhaseObjectifPaysRésultat
BB-031The purpose of this study is to evaluate the safety and tolerability of ascending doses (Part A) and selected doses (Part B) of BB-031 in acute ischemic stroke patients presenting within 24 hours of stroke onset. Participants will be randomized to receive one dose of either the investigational drug or placebo and will be followed for 90 days. A total of 228 patients are planned in this study. Accident vasculaire cérébral Phase 2 À vérifier United States, Australia, Canada À vérifier
BB-031The purpose of this study is to evaluate the safety and tolerability of ascending doses (Part A) and selected doses (Part B) of BB-031 in acute ischemic stroke patients presenting within 24 hours of stroke onset. Participants will be randomized to receive one dose of either the investigational drug or placebo and will be followed for 90 days. A total of 228 patients are planned in this study. Accident vasculaire cérébral Phase 2 À vérifier United States, Australia, Canada À vérifier

Essais cliniques

1
MoléculeIndication / populationPhaseNCTTitreStatut
BB-031 Accident vasculaire cérébral Phase 2 NCT06226805 Study of BB-031 in Acute Ischemic Stroke Patients (RAISE) RECRUITING

Publications

0
MoléculeIndication / populationTitreJournalDate
Aucune publication.