FDA clears Mesoblast Phase 2 clinical trial

Company News


Mesoblast Limited (ASX:MSB) has received regulatory clearance to start Phase 2 Clinical Trials on patients with active rheumatoid arthritis.
 
The US Food and Drug Administration (FDA) will now allow the regenerative medicine company to begin Phase 2 clinical trials of Mesenchymal Precursor Cells (MPCs). 
 
The randomized, double-blind placebo-controlled trial is expected to start in the second quarter of this year. 
 
Mesoblast’s chief says the company believes the broad immuneomodulatory effects of its Mesenchymal Precursor Cells could provide a tangible benefit to patients with debilitating autoimmune diseases, including rheumatoid arthritis.

Mesoblast booked a net loss of $71.1 million in the 2012 financial year. 

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