Who should not use peptides: the screening list
Active cancer, pregnancy and a known allergy rule peptides out. Several other conditions need a specialist first. Here is the list, and where each item comes from.
Only what has been tested in people: meta-analyses, randomised trials and other human studies. Switch on preclinical if you want the animal work too.
Active cancer, pregnancy and a known allergy rule peptides out. Several other conditions need a specialist first. Here is the list, and where each item comes from.
“Research use only” is a seller’s statement, not a legal category. In both countries regulators look at how a product is sold and used, and a disclaimer doesn’t settle that.
A big rat literature, three tiny uncontrolled human reports and one long-silent colitis trial. Here is exactly what has been tested in people.
Peer-reviewed trials show 24% weight loss at 48 weeks and large falls in liver fat; the headline 28% phase 3 figure is still company-reported.
In a six-week crossover trial of 24 healthy people aged 55 to 79, NR lifted NAD+ in blood cells and was well tolerated. Blood pressure hints were exploratory.
Every human study of follistatin-344 delivered the gene by viral vector into muscle, in a handful of patients. The protein sold in vials has no human data behind it.
Melanotan I, as afamelanotide, is approved for a rare light-sensitivity disease. Melanotan II was never approved, and case reports link it to changing moles and melanoma.
Only about 5% of treatments tested in animals end up approved for people. Here is why rodent results mislead, and a quick way to read any peptide abstract.
A certificate of analysis answers four separate questions: what is in the vial, how much, how clean, and how safe to inject. Most only answer one or two.
Two adults got intravenous BPC-157 on two consecutive days and had no side effects or blood-test changes. That’s all a two-person pilot can tell you.
Three small 12-week studies of the topical peptide OS-01 report better skin barrier and hydration. All were funded and authored by the company that owns it.
Bremelanotide is FDA-approved for low sexual desire in premenopausal women. In phase 3 it raised desire scores modestly, didn’t increase satisfying sexual events, and caused nausea in 40%.
An FDA advisory committee backed six of seven peptides for US pharmacy compounding, against its own scientists’ advice. The vote is not binding, and nothing is legal to compound yet.
The human trials used the full thymosin beta-4 protein, mostly as eye drops. TB-500, the seven-amino-acid fragment people inject, has no published human data at all.
Neither primary outcome improved in the larger of two published phase 2 trials. Some secondary measures did, and the drops looked safe for 28 days.
Kisspeptin is one of the better-studied peptides in humans, mostly by one London group. It can trigger egg maturation in IVF, but it is still experimental and unapproved.
Injected oxytocin reliably prevents bleeding after birth. The intranasal ‘trust hormone’ findings have failed to replicate, and the largest autism trial found no benefit.
Six months of daily tesamorelin cut visceral fat by 15.2% while placebo users gained 5.0%. Nearly half of users developed antibodies to the drug.
Both were once FDA-approved medicines, and both are now discontinued in the US. Their real track records are narrower, and more medical, than their current reputations.
Daily oral glutathione can raise body stores modestly. Skin-lightening effects are small, short-lived and based on a few trials, while IV glutathione has little evidence and a live contamination problem.
A copper peptide with decades of lab work and a few small human trials on skin and ulcers. Nobody has published a trial of injecting it.
Rodent studies were promising and six human trials found it well tolerated, but the largest trial failed on weight loss and development for obesity stopped in 2007.
Manufacturer-backed trials and pooled analyses report benefits; independent Cochrane reviews find no effect on stroke deaths and only very low-certainty gains in dementia.
The top dose took off 24.2% of body weight against 2.1% on placebo. It’s a striking number from a mid-sized, US-only trial with a generous way of counting.
In two phase 3 trials of 806 people with HIV, tesamorelin cut deep belly fat by about 15% more than placebo. The fat came back when it stopped, and nobody has run the trials people now cite it for.
Elamipretide is now an FDA-approved drug for one ultra-rare disease, on the strength of 12 patients. Its large trials in commoner conditions mostly missed their main goals.
LL-37 is central to innate immunity, but as a drug the evidence is thin: one small leg-ulcer trial looked good, and the larger follow-up failed.
Alone, cagrilintide cut weight by about 11% in 26 weeks; paired with semaglutide it reached 20% at 68 weeks, but lost a head-to-head against tirzepatide.
Three small phase 2 trials suggest it can regrow damaged small nerve fibres; the pain results are weaker, and there has never been a phase 3 trial.
In 17,604 adults with obesity and existing cardiovascular disease but no diabetes, semaglutide lowered major cardiac events from 8.0% to 6.5% over about three years.
Swiss trials in the 1980s reported better sleep with DSIP; the two independent placebo-controlled trials found little of clinical value. Nobody has found its gene or receptor.
Yes, a lot. Most peptides are destroyed or blocked in the gut, which is why nearly all peptide drugs are injected. Oral semaglutide is the exception, and it needed special engineering.
Oral NR and NMN reliably raise NAD+ in blood. Whether that makes anyone healthier is far less clear, and IV NAD+ drips have almost no trial evidence at all.
Ipamorelin reliably releases growth hormone, but its human record is a 1999 dosing study and a 2014 trial that missed its goal. No one has published a human study of it combined with CJC-1295.
At the top dose, people lost 20.9% of their body weight against 3.1% on placebo. Here is who was in the trial, what it cost them in side effects, and what it can’t tell you.
Around 20% average weight loss at 72 weeks, a head-to-head win over semaglutide, and heart-outcome data that matched rather than beat an older GLP-1 drug.
Semax is ACTH(4-7) with a Pro-Gly-Pro tail, which is why papers also call it an ACTH(4-10) analogue. Its human evidence is a few small, unblinded Russian stroke studies.
A licensed drug in some countries with thousands of trial patients behind it, but its biggest modern trials in sepsis and hepatitis C found no benefit.
Five controlled coeliac trials, one small positive signal at the lowest dose, and a Phase 3 stopped in 2022 because it wasn't going to work.
The human data on epitalon come from one research network, and they tested a pineal extract rather than the synthetic peptide itself. Independent work so far is limited to cells.
One version of CJC-1295 raised growth hormone for about a week in healthy adults. The other, sold as “no DAC”, has never been tested in people at all.
Weekly semaglutide cut body weight by 14.9% over 68 weeks against 2.4% on placebo. Most of that came back within a year of stopping.
About 15% weight loss at 68 weeks, fewer heart attacks and slower kidney decline in large trials, with stomach side effects, gallbladder risk and weight regain on stopping.
Selank’s human evidence is a handful of small Russian studies without placebo groups, most from the team that made it. Promising on paper, unproven by any independent standard.
Seven questions that sort a real finding from a weak one: who was studied, how many, compared with what, measured how, for how long, and who paid.