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The second group comprises non-glutathione disulfide substrates (RS 2 or RSSR) that are reduced by two molecules of GSH, yielding one dithiol product or two monothiol products (R(SH) 2 or RSH + RSH) and GSSG (Fig

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Assuming Eli Lilly follows a similar timeline to tirzepatide, the earliest possible FDA approval for retatrutide would likely occur in late 2027 or 2028, depending on Phase 3 trial results and regulatory review timelines