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» FDA clears Egret's EGT-101 to enter clinic for delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage
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Neurology/Psychiatric
FDA clears Egret's EGT-101 to enter clinic for delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage
Feb. 6, 2023
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Egret Therapeutics, a portfolio company of Turret Capital Management LP, has announced FDA clearance of its IND application for EGT-101 for the treatment of delayed cerebral ischemia following aneurysmal subarachnoid hemorrhage.
BioWorld Science
Neurology/psychiatric
FDA
IND