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Canadians currently have access through clinical trial participation or research peptide suppliers while awaiting official approval
B12 shots, the key difference lies in the ingredients
Melanotan II itself was never taken through completed late-stage efficacy and safety trials and was never approved
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In ACCESS II, across all active arms in participants who reached doses 120 mg or higher from 28 to 44 weeks, there was only one (3.7%) adverse event (AE)-related treatment discontinuation
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