Abstract
Serotonin agonists can reduce glutamate-induced excitotoxicity in cerebral ischemia. The potent 5- HT1A agonist BAY x 3702, or repinotan, has reduced cortical infarct volume in pre-clinical models even when given 5 hours after injury. Early clinical trials showed that the drug was safe, and displayed primarily serotonergic side effects such as nausea and vomiting. A phase IIb trial in moderate to moderately severe strokes completed enrollment in June 2004.
Keywords: Infarct, ischemia, acute stroke treatment, neuroprotection, neuroprotectant, repinotan
Current Drug Targets - CNS & Neurological Disorders
Title: Repinotan, A 5-HT1A Agonist, in the Treatment of Acute Ischemic Stroke
Volume: 4 Issue: 2
Author(s): Helmi L. Lutsep
Affiliation:
Keywords: Infarct, ischemia, acute stroke treatment, neuroprotection, neuroprotectant, repinotan
Abstract: Serotonin agonists can reduce glutamate-induced excitotoxicity in cerebral ischemia. The potent 5- HT1A agonist BAY x 3702, or repinotan, has reduced cortical infarct volume in pre-clinical models even when given 5 hours after injury. Early clinical trials showed that the drug was safe, and displayed primarily serotonergic side effects such as nausea and vomiting. A phase IIb trial in moderate to moderately severe strokes completed enrollment in June 2004.
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Cite this article as:
Lutsep L. Helmi, Repinotan, A 5-HT1A Agonist, in the Treatment of Acute Ischemic Stroke, Current Drug Targets - CNS & Neurological Disorders 2005; 4 (2) . https://dx.doi.org/10.2174/1568007053544165
DOI https://dx.doi.org/10.2174/1568007053544165 |
Print ISSN 1568-007X |
Publisher Name Bentham Science Publisher |
Online ISSN 1568-007X |
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