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Marsha Blackburn and Tennessee Attorney General Jonathan Skrmetti are urging the Federal Trade Commission to investigate potentially dangerous, misleadingly advertised GLP-1 drugs

The blend is not approved for human use Tesamorelin alone is FDA-approved as EGRIFTA for HIV-associated lipodystrophy, while Ipamorelin is not FDA-approved for any indication

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Liraglutide-treated patients had also a lower risk of death from cardiovascular causes and from any cause [32]

Compared with placebo, ziltivekimab reduced hsCRP concentrations by up to 92%, prompting the formal cardiovascular outcome trial, ZEUS (NCT05021835)

Ongoing Surveillance During Treatment Once peptide therapy is initiated, ongoing surveillance for malignancy should continue throughout the treatment period and potentially beyond, depending on treatment duration and individual risk factors