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Recruiting Phase 2 Interventional

A Study of TAK-755 in Adults With Acute Ischemic Stroke

ClinicalTrials.gov ID: NCT07392450

Public ClinicalTrials.gov record NCT07392450. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 12:20 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety, Tolerability, and Efficacy of TAK-755 in Acute Ischemic Stroke

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Acute ischemic stroke (AIS) is a medical emergency that happens because of a sudden stop of blood flow to a part of the brain. This happens when a blood clot forms within the vessel (known as thrombotic occlusion) or a clot originating from somewhere else blocks a blood vessel (known as embolic occlusion). Strokes can cause serious health problems, death, and affect one's quality of life. To reduce long-term damage, it is important to restore blood flow to the brain as soon as possible. The main aim of this study is to check how safe TAK-755 is, and how well adults with AIS tolerate it. Other aims are to check how well TAK-755 helps participants to manage their everyday activities and to understand whether it helps reduce the seriousness of their stroke symptoms when compared to placebo. A placebo looks like TAK-755, but does not have any medicine in it, to make sure participants do not know which treatment they are taking. The participants will receive TAK-755 or placebo once; afterwards, their health will be monitored for about 3 months (90 days). All participants, regardless of their assignment to either TAK-755 or placebo, will receive the usual treatment for AIS as per the hospital's normal practice.

Study identification

NCT ID
NCT07392450
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
222 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 16, 2026
Primary completion
Dec 5, 2027
Completion
Dec 5, 2027
Last update posted
Aug 13, 2026

2026 – 2027

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
HonorHealth Neurology Scottsdale Arizona 85251 Recruiting
University of Arizona Tucson Arizona 85724 Not yet recruiting
University of California San Francisco San Francisco California 94143 Not yet recruiting
Massachusetts General Hospital Boston Massachusetts 02114 Not yet recruiting
University at Buffalo Buffalo New York 14202 Not yet recruiting
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 Not yet recruiting
Vanderbilt University Medical Center Nashville Tennessee 37232 Not yet recruiting
HCA Houston Healthcare - North Cypress Cypress Texas 77429 Not yet recruiting
Neurology Consultants of Dallas, PA Dallas Texas 75243 Not yet recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 51 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07392450, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2026 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07392450 live on ClinicalTrials.gov.

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