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Robert F. Kennedy Jr. Discusses Peptide Restrictions on Joe Rogan | Jon Eaton, ACHE, MBA posted on the topic | LinkedIn

For a compound to progress from its current status to FDA approval, it would need to complete IND-enabling studies (including formal toxicology and GMP manufacturing), a Phase 1 safety trial in humans, Phase 2 efficacy and dose-finding trials, and Phase 3 confirmatory trials — a process that typically takes 8 to 15 years and costs hundreds of millions of dollars with no guarantee of success

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This might be due to the fact the SnCE1 tetramer being of moderate stability existing in an equilibrium with a monomeric state as shown by analytical SEC