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ATTAIN-1 (orforglipron, 72 weeks): Discontinuation due to AEs: 5.3-10.3% (orforglipron) vs 2.7% placebo Key characteristics: GI profile is broadly similar to injectable GLP-1 agonists despite oral route Nausea rates are comparable to tirzepatide The oral formulation does not appear to worsen GI tolerability relative to SC injection Safety profile described as "consistent with injectable GLP-1 medicines" Ecnoglutide# Ecnoglutide is a cAMP-biased GLP-1 receptor agonist developed by Sciwind Biosciences

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It is for this reason that I have found intravenous (IV) administration of GSH to have significant and rapid clinical effects in neurological diseases

This type of toxicity may be exhibited by cyclosporine