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Cabaletta Bio Receives FDA Clearance of IND Application for CABA-201 for Treatment of Systemic Lupus Erythematosus

Cabaletta Bio Receives FDA Clearance of IND Application for CABA-201 for Treatment of Systemic Lupus Erythematosus
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Cabaletta Bio Reports Fourth Quarter and Full Year 2022 Financial Results and Provides Business Update

16.03.2023 - – Company expecting Investigational New Drug (IND) clearance in the first half of 2023 for CABA-201, a 4-1BB-containing fully human CD19-CAR T cell therapy, with potential to generate initial clinical data by the first half of 2024 – PHILADELPHIA, .

Form S-3 Cabaletta Bio, Inc

Form S-3 Cabaletta Bio, Inc
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