Participate in Research

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
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
-Adults ages 18+.
-Have been diagnosed with a stroke or stroke symptoms.
-Please contact the research team for other eligibility criteria.
Age Group: Adults Open Study
Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, then reach out to the study team directly at the contact information above and someone will assist you.

Your information will be shared only with the research study team and administrative staff for recruitment and will remain confidential. Your information will be stored until study recruitment is closed. Should you no longer want this information to be provided in the aforementioned ways, please contact the study team directly.

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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