Trial Number
471-24
Condition
Stroke
Participant Age Range
18 years and older
Participant Gender
Any
Enrolling Participants
Yes
Overview
“A multicenter, double-blinded, placebo-controlled, single ascending dose, two-part, randomized clinical trial to assess safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of BB-031 in acute ischemic stroke (AIS) patients”
The 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.