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Significant degradation has likely occurred over 8 to 12 hours at room temperature

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Human clinical trial data remains limited, but the mechanistic and preclinical evidence base is stronger for gut-related peptides than for most other peptide research categories

Based on these data, the FDA approved tesamorelin (marketed as EGRIFTA) for the reduction of excess abdominal fat in HIVassociated lipodystrophy, not as a general weightloss drug for the wider population. Tesamorelin Risks and Considerations Like all hormonemodulating therapies, tesamorelin carries potential risks, including fluid retention, joint pain, injectionsite reactions, and effects on glucose metabolism in susceptible patients