FDA label
Tested in controlled human trials and reviewed by the FDA for a specific product, use, and population. Example: the semaglutide and tirzepatide escalation schedules.
READ RESEARCH BETTER
A biological mechanism may be interesting without demonstrating that a product is safe or effective in people. Ask where the evidence sits, how large the study was, what it measured, and whether the product studied matches the product being sold.
For educational purposes only. Not medical advice, diagnosis, treatment, or prescribing guidance. Research and regulatory information can change over time.
WHERE NUMBERS COME FROM
Protocol charts often mix FDA-labeled doses with numbers repeated online, and present both the same way. Before trusting a number, ask where it came from.
Tested in controlled human trials and reviewed by the FDA for a specific product, use, and population. Example: the semaglutide and tirzepatide escalation schedules.
Doses studied in a registered, peer-reviewed trial, but not approved. Example: retatrutide 1–12 mg and eloralintide 1–9 mg weekly in Phase 2.
Labeled in another country, such as thymalfasin (thymosin alpha-1) or Semax. Useful context, but not a U.S. approval and not always based on large trials.
Ranges repeated on forums, protocol cards, and seller pages without a controlled human trial behind them. Repetition is not evidence. Pep Guide does not publish these.
Large trials often report two results. The treatment-policy number counts everyone, including people who stopped. The efficacy number counts only people who stayed on treatment, so it is higher. CagriSema’s 20.4% and 22.7% come from the same trial.
“20% average weight loss” means some people lost much more and some much less. Trial results describe groups of screened participants under monitoring, not what will happen to any one person.