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Mesoblast (MESO) Notified by FDA that Available Data from Phase 3 Trial Appear Sufficient to Support BLA Submission

Mesoblast (MESO) Notified by FDA that Available Data from Phase 3 Trial Appear Sufficient to Support BLA Submission
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United States Food & Drug Administration (FDA) Supports Accelerated Approval Pathway for Rexlemestrocel-L in End-Stage Heart Failure Patients with a Left Ventricular Assist Device (LVAD)

11.03.2024 - NEW YORK, March 10, 2024 (GLOBE NEWSWIRE) - Mesoblast Limited (Nasdaq:MESO; ASX:MSB), global leader in allogeneic cellular medicines for inflammatory diseases, today announced that U.S. FDA supports an accelerated approval pathway for . Seite 1

Mesoblast (MSB) FDA Supports Accelerated Approval Pathway for Rexlemestrocel-L

Mesoblast (MSB) FDA Supports Accelerated Approval Pathway for Rexlemestrocel-L
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