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Mesoblast Receives FDA Clearance For Phase 2 Clinical Trial Of Mesenchymal Precursor

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Trial will be randomized, double-blind placebo-controlled dose escalation study to evaluate the safety, tolerability and effectiveness of a single intravenous infusion of two MPC dose levels over an initial period of 3 months in patients who have had poor or incomplete responses to biologic inhibitors of the TNF-alpha pathway Regenerative medicine company Mesoblast Limited (...

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