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Timeless Study for Stroke
Protocol: SITE00000111
Full Title
A phase III, Prospective, Double-Blind, Randomized, Placebo-Controlled Trial of Throbolysis in imaging-eligible, late-window patients to assess the efficacy and safety of tenecteplase
Description
This study enrolls adults who have had a recent stroke or stroke symptoms. The purpose of this study is to compare how well the study drug (tenecteplase) works for people with stroke symptoms.

You will be in this study for about 3 months and complete two 90-minute visits during that time. You will be randomized (like flipping a coin) to take either the study drug (tenecteplase) or a placebo. A placebo looks like the study drug but has no active ingredients. You will also have the current standard of care for stroke. Study takes place at Buffalo General, Gates Vascular Institute, and UBMD Neurology locations.
Compensation: No
Eligibility
-Adults ages 18+.
-Have been diagnosed with a stroke or stroke symptoms.
-Please contact the research team for other eligibility criteria.
Age Group: Adults
ClinicalTrials.gov: Open Study

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Thank you for your interest. This study has restricted recruiting for participants and is not accepting inquiries at this time. If you are interested in learning more about studies at UB, you can sign up for the Buffalo Research Registry.
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