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.

Provider

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