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The primary analysis was based on the dose assigned at randomization (planned treatment) and included data censored for COVID-19-related discontinuations, while a sensitivity analysis used the actual maintenance dose received (actual treatment) with on-treatment data only

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Some of those who have used injectable peptides unapproved for US sale from unregulated suppliers on the gray market have reported concerns, including unwanted changes to skin pigmentation, infection, swelling, pain, redness, and new or changing moles. Addressing safety concerns, the APC CEO reports that there has not been an uptick in adverse events reported through the FDAs adverse events reporting database related to injectable peptides