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2022.03.25

Taiwan FDA Approved the Phase 2 IND for Multiple-dosing of LT3001

Lumosa is proud to announce the approval of Phase 2, multi-dose trial of LT3001 in patients with acute ischemic stroke by Taiwan FDA. The company will soon initiate the multi-national, multi-site study, in the US and Taiwan. The trial will enroll 200 patients with disabling acute ischemic stroke within 24 hours of stroke symptom onset or last known well.