Today's digest underscores the growing tension between peptide accessibility and safety. ProPublica published a major investigation warning that the FDA's reversal on 14 restricted peptides could flood the market with inadequately tested drugs — a concern punctuated by a federal indictment of a Utah physician who sold misbranded Chinese peptides to over 200 patients. On the clinical side, a randomized trial of semaglutide for major depression produced intriguing but inconclusive results: no improvement in executive function, but signals of benefit in global cognition. Meanwhile, the GLP-1 story continues to expand beyond metabolic disease, with a comprehensive NeurologyLive review mapping the repositioning of GLP-1 drugs for Alzheimer's, Parkinson's, and other neurological conditions. In the business arena, Noom's acquisition of Tailor Made Compounding signals that tech-wellness platforms are moving aggressively into peptide-based therapies, even as NBC News published a widely-read investigation questioning whether the peptide craze is outpacing the science.