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Completed Phase 3 Interventional

Safety and Effectiveness of NXY-059 for the Treatment of Patients Who Have Suffered From a Stroke

ClinicalTrials.gov ID: NCT00061022

Public ClinicalTrials.gov record NCT00061022. 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 Oct 21, 2026, 9:55 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

SAINT (Stroke - Acute Ischemic - NXY Treatment) A Double Blind, Randomized, Placebo Controlled, Parallel Group, Multicenter, Phase IIb/III Study to Assess the Efficacy and Safety of Intravenous NXY-059 in Acute Ischemic Stroke

Brief summary

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

This study will determine if NXY-059 will improve recovery from an acute stroke. The study is designed to look at both overall recovery and recovery of motor function, for example muscle strengthen and coordination.

Study identification

NCT ID
NCT00061022
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
3,200 participants

Conditions and interventions

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 2003 (Type not available)
Primary completion
Sep 2006 (Actual)
Completion
Sep 2006 (Actual)
Last update posted
Nov 15, 2010

2003 – 2006

United States locations

U.S. sites
98
U.S. states
33
U.S. cities
98
Facility City State ZIP Site status
Research Site Birmingham Alabama — —
Research Site Phoenix Arizona — —
Research Site Fort Smith Arkansas — —
Research Site Arcadia California — —
Research Site Concord California — —
Research Site Englewood California — —
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Research Site Lane Panama City Florida — —
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Research Site Marrero Louisiana — —
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Research Site Pontiac Michigan — —
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Research Site Edison New Jersey — —
Research Site Long Branch New Jersey — —
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Research Site Ridgewood New Jersey — —
Research Site Summit New Jersey — —
Research Site Toms River New Jersey — —
Research Site Trenton New Jersey — —
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Research Site Flushing New York — —
Research Site New Hyde New York — —
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Research Site Asheville North Carolina — —
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Research Site Durham North Carolina — —
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Research Site Olympia Washington — —
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Research Site Tacoma Washington — —
Research Site Charleston West Virginia — —
Research Site Madison Wisconsin — —
Research Site Marshfield Wisconsin — —
Research Site Milwaukee Wisconsin — —

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 158 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00061022, 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 Nov 15, 2010 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00061022 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →