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A Study to Evaluate the Efficacy and Safety of BIIB131 for Participants With Ischemic Stroke Between 4.5 and 24 Hours After Last Known Well

← catalyst calendar

NCT05764122

Sponsored by Biogen (industry) · BIIB — their whole pipeline →.

Phase
Phase 2
Status
Withdrawn
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
0actual

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Sponsor decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-03-29estimatedWhen the study began enrolling
Primary completion2025-07-07estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-07-07estimatedThe whole study's end, after follow-up
First posted2023-03-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-02-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Ischemic Stroke

Interventions

  • Drug: BIIB131
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Part 1: Percentage of Participants with Arterial Revascularization
measured Up to 6 hours
Part 1: Percentage of Participants with Reperfusion of the Ischemic Field
measured Up to 6 hours
Part 2: Ordinal Modified Ranking Scale (mRS) Score Based on a 6-Point Ordinal Scale
measured Day 90

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