FDA Approves TNKase for Acute Ischemic Stroke
- The U.S. Food and Drug Administration has approved TNKase for treating acute ischemic stroke in adults.
- TNKase is given as a single five-second intravenous bolus, which is faster than the current standard treatment, Activase .
- Genentech's new 25-mg vial of TNKase will be available in the coming months, following the approval.
- Approval was based on a study showing TNKase's efficacy and safety were comparable to Activase.
31 Articles
31 Articles
FDA Approves TNKase for Acute Ischemic Stroke
THURSDAY, March 6, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved TNKase (tenecteplase), a thrombolytic or clot-dissolving agent, for the treatment of acute ischemic stroke in adults.
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.flex_column.av-pxfofs-f8cffa300d0abe60229a0238b37e998b{ border-radius:0px 0px 0px 0px; padding:0px 0px 0px 0px; } 07/03/2025/in ESO, Stroke Research /by Carine Legio Authors: Dr. Alexandru Dimancea X: @DimanceaAlex Dr. Raoul Pop X: @RaoulPop25 Recent research efforts in the field of stroke interventional treatment have focused on efficacy and safety of mechanical thrombectomy (MT) in medium vessel occlusions (MeVO)-acute ischaemic stroke (AIS)…
A 'PACT' to monitor stroke in real-time
Every year, millions of people die from stroke. In order to win against this disease which occurs the moment when a blood vessel is blocked in brain, a research team from the Pohang University of Science & Technology (Postech) made a breakthrough with a new technology combining light and sound.
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