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Demand continues to grow despite ongoing questions about: Human clinical trials Evidence of efficacy Appropriate dosing Long-term safety Product quality Compounding standards Supply-chain integrity For providers, the meeting may offer clues about how regulators view these challenges and whether future guidance could affect access to compounded peptide therapies

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Patients were excluded if they were pregnant, immunocompromised, had leukopenia, hematologic malignancies, or were transitioning to palliative care