Corporate
2025.11.28
Lumosa Has Received Feedback for the Type C Consultation from the US FDA
The Company submitted a Type C meeting request to the US FDA for LT3001, a novel therapy for acute ischemic stroke, based on the existing nonclinical data and clinical trial results.
Corporate
2025.11.04
Beach Cleanup!
Corporate
2025.10.28
Lumosa Share Positive P2 Trial Results
LUMOSA THERAPEUTICS ANNOUNCES POSITIVE RESULTS FROM LT3001 (INTRAVENOUS ODATROLTIDE) PHASE 2B CLINICAL TRIAL IN ACUTE ISCHEMIC STROKE
Corporate
2025.10.17
Announcement: Change in Company Spokesperson
Corporate
2023.09.26
Lumosa's LT1001 Receives Approval from Brunei
Expanding its presence in Southeast Asian market
Corporate
2023.07.26
LT3001 Received Formulation Patent from USPTO