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» Uniqure’s AMT-260 gene therapy cleared by FDA to enter clinic for mesial temporal lobe epilepsy
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Neurology/Psychiatric
Uniqure’s AMT-260 gene therapy cleared by FDA to enter clinic for mesial temporal lobe epilepsy
Sep. 5, 2023
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Uniqure NV has received FDA clearance of its IND application for AMT-260, the company’s gene therapy candidate that represents a potential one-time administered approach to treating refractory mesial temporal lobe epilepsy (MTLE).
BioWorld Science
Regulatory
Neurology/psychiatric
Gene therapy
FDA
IND
