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Its pivotal trial enrolled 816 participants and met its primary efficacy endpoint, supporting FDA approval in 2010 with documented visceral fat reductions of roughly 15-18% over 26 weeks

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Cloudy solution after reconstitution suggests potential contamination or degradation

The oral bioavailability and blood-brain barrier penetration are what distinguish Dihexa from most neuropeptides (which require intranasal or IV delivery)

A Canadian company, Replicel, is running clinical trials for their autologous cell therapy tendinopathy treatment called RCT-01