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Climb Bio Reports Fourth Quarter and Year-End 2024 Financial Results and Provides Business Updates

Received Clearance from the U.S. Food and Drug Administration (FDA) for Clinical Trials of Budoprutug in Primary Membranous Nephropathy (pMN), Immune Thrombocytopenia (ITP), and Systemic Lupus Erythematosus (SLE) Completed Studies to Support Process Optimization through Cell Line Switch for Budoprutug and Filed Additional Patent Applications to Further Strengthen Intellectual Property Position Expanded Pipeline to Include CLYM116, an Anti-APRIL (A PRoliferation-Inducing Ligand) Monoclonal Antibo

articleClimb Bio, Inc.March 25, 202511/company/climb-bio-inc/news/climb-bio-reports-fourth-quarter-200500632
Climb Bio Reports Fourth Quarter and Year-End 2024 Financial Results and Provides Business Updates

About this update from Climb Bio, Inc.

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More updates from Climb Bio, Inc.

the companyClimb Bio, Inc.clinical trialsClimb Biomonoclonal antibodyDr. BrennanFDA Clearance