A plain-language overview of what peptides are, which peptide medicines have approved uses, what off-label and compounded mean, what remains investigational, and how a supervised consultation actually works.
Status describes regulation, not effectiveness. A substance can be investigational and still be studied seriously; it can also be widely marketed and still lack human evidence.
| Substance | Regulatory status | Human evidence | Guide |
|---|---|---|---|
| Semaglutide | Approved | Large randomized human trials for its approved indications | Read guide |
| Tirzepatide | Approved | Large randomized human trials for its approved indications | Read guide |
| Sermorelin | Approved | Formerly FDA-approved for growth failure in children; withdrawn 2009 | Read guide |
| PT-141 (bremelanotide) | Approved | Approved for one specific indication in one population | Guide in review |
| Retatrutide | Investigational | Largest phase 3 weight losses recorded; no approval, and FDA bars compounding | Read guide |
| Ipamorelin | Investigational | Only human efficacy trials were in postoperative ileus; the published one missed its endpoint | Read guide |
| CJC-1295 | Investigational | Only efficacy trial was terminated in 2006 without results | Read guide |
| BPC-157 | Investigational | Largely animal and in-vitro; FDA evaluated it for ulcerative colitis, not tendon repair | Read guide |
| TB-500 | Investigational | No completed human trial has ever tested it; cited research used a different molecule | Read guide |
| GHK-Cu | Investigational | Two topical human trials, neither beat placebo; no injectable trial exists | Read guide |
Peptides are short chains of amino acids. Some are approved medicines with decades of trial data behind a specific use. Others exist only as research materials with no approved human indication. The word covers both, which is exactly why the label on a page matters more than the category name.
A clinician may legally prescribe an approved medicine for a use outside its approval when they judge it appropriate. Off-label is not a loophole and not an endorsement: the strength of evidence for the specific off-label use is the thing to ask about.
A compounding pharmacy prepares a medicine for an individual patient. Compounded drugs are not FDA-approved and are not reviewed by the agency for safety, effectiveness or manufacturing quality. Ask which pharmacy prepares it and how that pharmacy is licensed.
A pharmacy dispenses on a prescription under state and federal oversight. A research supplier sells materials labeled for laboratory use only, and a research-use disclaimer does not make a product appropriate for a person. Documentation published by a seller is not a substitute for the oversight a prescription carries.
Published prices generally cover consultation and program fees. Medication, laboratory work and follow-up are frequently billed separately. Our city pages record what clinics publish, with the date observed; anything below three disclosed sources is reported as insufficient rather than estimated.