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A Study of ASP2246 for People Who Have Movement Problems Caused by Brain Injury After a Stroke

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NCT07318714 · readout in 1,288 d

Sponsored by Astellas Pharma Inc (industry) · 4503.T — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
84estimated
Sites
5
Country
Japan

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

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-04-03actualWhen the study began enrolling
Primary completion2030-02-28estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-02-28estimatedThe whole study's end, after follow-up
First posted2026-01-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-09actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Chronic Ischemic Stroke

Interventions

  • Drug: ASP2246
  • Procedure: Brain surgery
  • Procedure: Sham surgery
  • Other: Rehabilitation therapy

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with Dose-Limiting Toxicity (DLT)
measured Up to 2 Weeks
Number of participants with Treatment-Emergent Adverse Events (TEAEs)
measured Up to 52 Weeks
Number of participants with Serious Adverse Events (SAEs)
measured Up to 52 Weeks
Number of participants with an Adverse Event of Special Interest (AESI)
measured Up to 52 Weeks
Number of Participants with Suicidal Ideation and/or Behavior as Assessed by Columbia-Suicide Severity Rating Scale (C-SSRS)
measured Up to 52 Weeks

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