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NAD+ research-grade peptide, third-party tested with COA available (99%+ purity)

Statistical analyses Patients were followed from initiation of the study drugs (after 1 January 2007) until first diagnosis of prostate cancer or other cancer (except non-melanoma skin cancer), emigration, death or 31 December 2019

Recently, the FDA has placed this peptide under strict evaluation regarding its use in human drug compounding, as the agency requires more large-scale data to fully confirm its long-term safety and effectiveness