| http://www.w3.org/ns/prov#value | - e FDA or other regulatory agencies to require additional nonclinical or clinical studies prior to initiation of the planned Phase 2 clinical study of MST-188 in acute limb ischemia; the risk that, even if clinical studies are successful, the FDA or other regulatory agencies may determine they are not sufficient to support a new drug application; the Company's reliance on contract research organiza
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