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Peptideworth

Compounds

Every peptide we’ve graded

One page per molecule: what it is, how it’s supposed to work, what has actually been tested in a human for the use it’s sold for, and what a reader should not assume from that. No scores out of ten — an evidence tier, printed the same way on every compound.

Peptides graded

13

FDA-approved

4

RCT evidence

6

The compounds

Compounding restricted

BPC-157

BPC-157 is sold for tendon, gut, and muscle healing on the strength of rodent studies. Here is what those studies found, and why no human trial backs it yet.

Evidence strength

Evidence strength: Animal only

FDA-approved

Bremelanotide (PT-141)

Bremelanotide is FDA-approved as Vyleesi — for premenopausal women only. The label says it is not indicated in men. Here is what the trials measured.

Evidence strength

Evidence strength: Randomized trials

Research use only

Cagrilintide

Cagrilintide's famous numbers belong to CagriSema, the combination with semaglutide. Alone, its published record is one 26-week phase 2 dose-finding trial.

Evidence strength

Evidence strength: Early human

Compounding restricted

GHK-Cu

Every human trial of GHK-Cu is topical, and both were null on their objective endpoints. The FDA has drawn its line at exactly the injectable route.

Evidence strength

Evidence strength: Early human

Compounding restricted

Glutathione

Glutathione is sold as an injection for skin and energy. The randomized skin evidence is oral and topical, and the injected record is one 21-person pilot.

Evidence strength

Evidence strength: Early human

Compounding restricted

NAD+

Injected NAD+ has one randomized trial — 10 mg a day for a week, in heart failure patients. The large human literature is on oral precursors instead.

Evidence strength

Evidence strength: Early human

Research use only

Retatrutide

The 24.2% is a phase 2 result from one 12 mg arm. One phase 3 has published — 15.3% at 40 weeks in type 2 diabetes. Four more finished unreported.

Evidence strength

Evidence strength: Early human

FDA-approved

Semaglutide

Semaglutide has the longest outcomes data in the class — 17,604 patients, 39.8 months. Its newest indication, MASH, is accelerated approval on interim data.

Evidence strength

Evidence strength: Randomized trials

Compounding restricted

Sermorelin

Sermorelin has 19 randomized trials, all from 1986 to 2005, and none measured aging, body composition or sleep. Here is what they did measure.

Evidence strength

Evidence strength: Randomized trials

Research use only

Survodutide

Survodutide's phase 2 reached 14.9% at 46 weeks. Its phase 3, at a higher dose over 76 weeks, reached 13.0% — with placebo at 5.4%. Not FDA-approved.

Evidence strength

Evidence strength: Randomized trials

Research use only

TB-500

TB-500 is a seven-residue fragment of thymosin beta-4, not the protein itself. The human trials people cite used the full protein, mostly as an eye drop.

Evidence strength

Evidence strength: Animal only

FDA-approved

Tesamorelin

Tesamorelin is FDA-approved — for visceral fat in HIV-associated lipodystrophy. Its label says it is not indicated for weight loss and is weight-neutral.

Evidence strength

Evidence strength: Randomized trials

FDA-approved

Tirzepatide

Tirzepatide's 20.9% is the 15 mg arm of a 2,539-person trial. Approved for weight and sleep apnea; its outcomes trial showed noninferiority, not superiority.

Evidence strength

Evidence strength: Randomized trials

Looking for a goal, not a molecule?

This page is organized by compound. If you already know what you’re trying to change — sleep, injury recovery, a weight-loss plateau — the goal pages rank every relevant compound against that one outcome instead.

How a claim is graded, and what moves a compound between evidence tiers, is on our methodology page.

Medical disclaimer: This content is for general educational purposes only and is not medical advice, diagnosis, or treatment. Always consult a licensed healthcare professional before starting, stopping, or changing any treatment.