No…quite the opposite
Answered most non-holders issues
Also my impression is they read HC and made a point of countering
*Trial end point design in the Phase 3 trial
*Use of HA as a control and then as a carrier for the MSC’s
*Potency assays and use of data sets gleaned from both Rem-l and Rex-l for use in upcoming applications to FDA
*Future funding is being explored
Chronic Lower Back Pain - the sleeping giant., page-153
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