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Future: Dedicated NASH Phase 3 Trial - NOT YET STARTED Status: Expected 2027-2030 (after obesity/diabetes approval) What This Would Include: Liver biopsy as PRIMARY endpoint NASH resolution as primary outcome Fibrosis improvement measurement Required for FDA approval specifically for NASH indication Why Wait
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The cost asymmetry that makes bac water choice consequential GLP-1 vial prices put more dollars at risk per reconstitution than typical research peptides
These effects include the reduction of inflammation and oxidative stress, vasodilation, decreased arterial stiffness, and a reduction in myocardial fibrosiskey factors in the pathophysiology of HFpEF
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