Peptides for weight loss
Every compound on the site sold or studied for weight loss, from the approved GLP-1 drugs to alternatives with little human data.
Most of the weight loss anyone can point to on this page comes through one hormone. GLP-1 drugs such as semaglutide and tirzepatide have large trials, approved weight-loss products and years of prescribing behind them, and their results are the reason every other compound here gets asked about.
The page is split into three sections because the evidence splits that way. The GLP-1 section holds the approved drugs and the newer multi-receptor compounds built to beat them. The amylin section holds analogs of amylin, a second fullness hormone that acts on a separate pathway and is often paired with a GLP-1 in newer drugs. The last section holds everything else sold for fat loss, where the human data is thin and in some cases negative.
Before comparing anything, check the badge on each card. A drug approved for weight loss, a drug approved for something else and a compound never tested in a person can sit next to each other on this page.
GLP-1 agonists
Compounds that copy GLP-1, the gut hormone released after a meal that tells your brain you have eaten.
Retatrutide is a triple agonist that switches on three hormone receptors at once: GLP-1, GIP, and glucagon. In plain terms: it copies three of your natural 'I'm full' and fat-burning signals together, which is why it drives some of the largest weight-loss numbers seen in trials. It is still experimental.
Tirzepatide is a dual agonist that activates two gut-hormone receptors at once, GLP-1 and GIP. In plain terms: it works on two of your body's appetite-and-blood-sugar signals together, which tends to produce more weight loss than drugs that hit only one. It is the active drug in Mounjaro and Zepbound.
Semaglutide is a GLP-1 receptor agonist, a lab-made copy of a natural gut hormone your body releases after eating. In plain terms: it flips on your 'I'm full' signal, so you feel satisfied sooner, eat less, and your blood sugar steadies. It is the active drug in Ozempic and Wegovy.
Survodutide is a dual GLP-1 and glucagon agonist. In plain terms: it copies your fullness signal and also nudges your metabolism to burn more energy, which is why trials show strong weight loss and better fatty liver. It is still experimental.
Mazdutide is a dual GLP-1 and glucagon agonist, similar in design to survodutide. In plain terms: it works on appetite and metabolism at once for weight loss and better blood sugar. It is approved in China and still in trials elsewhere.
Orforglipron is an oral GLP-1 receptor agonist, and unlike most of this group it is a small molecule rather than a peptide, so it survives digestion as a pill. In plain terms: it gives the same appetite control as the injectable GLP-1 drugs without needles, and unlike earlier oral versions it does not need to be taken on an empty stomach.
This blend puts retatrutide and cagrilintide in one vial. In plain terms: it copies the CagriSema idea of pairing a gut-hormone drug with an amylin analogue, except neither half of this pairing is approved and the combination has never been trialled.
CagriSema is a fixed combination of cagrilintide (an amylin copy) and semaglutide (a GLP-1 copy) in one weekly shot. In plain terms: it hits two separate fullness pathways at once for bigger weight loss than either alone. It is still experimental.
Liraglutide is a GLP-1 receptor agonist, the same hormone-copying approach as semaglutide but shorter-acting, so it is taken daily. In plain terms: it turns up your fullness signal to curb appetite and steady blood sugar. It is the drug in Saxenda and Victoza.
Albiglutide was a weekly GLP-1 receptor agonist approved in 2014. In plain terms: it worked, it was less effective than its rivals, it needed mixing before every injection, and its maker pulled it worldwide.
Amycretin is a single molecule that combines GLP-1 and amylin activity. In plain terms: it packs two different 'stop eating' signals into one compound, with strong early weight-loss data. It is still experimental, in pill and injectable forms.
Beinaglutide is a recombinant human GLP-1 approved in China. In plain terms: unlike semaglutide and the rest, it is not a modified analogue. It is the human hormone itself, which is why it has to be injected three times a day.
CT-388 is a dual GLP-1 and GIP agonist, the same two-receptor family as tirzepatide. In plain terms: it works on two appetite-and-blood-sugar signals for weight loss. It is a weekly shot still in trials.
Danuglipron is an oral GLP-1 receptor agonist and a small molecule, not a peptide, so it works as a pill. In plain terms: it gives GLP-1-style appetite control without injections. It is in testing.
Dulaglutide is a GLP-1 drug, the same family as Ozempic. It copies a gut hormone that tells the pancreas to release insulin when blood sugar is high, and slows how fast the stomach empties. In plain terms: it lowers blood sugar and takes the edge off hunger. It is approved for type 2 diabetes only, and the weight loss is much smaller than what people expect from this drug family.
Ecnoglutide is a once-weekly GLP-1 receptor agonist developed by Sciwind Biosciences in Hangzhou. It is described as cAMP-biased, meaning it drives one arm of the receptor's signalling while producing much less receptor internalisation than semaglutide.
Exenatide was the first GLP-1 drug ever approved. It is a copy of a substance found in the saliva of the Gila monster, a venomous lizard, which turned out to act on the same receptor as the human gut hormone GLP-1 while lasting much longer. In plain terms: this is where the whole Ozempic family started. It is still approved, but it has largely been left behind by newer drugs that work better and are taken less often.
Lixisenatide is a daily GLP-1 receptor agonist approved for type 2 diabetes. In plain terms: it is a real approved drug from the same family as semaglutide, and it was outsold and withdrawn from the US market.
MariTide is an unusual design, an antibody linked to two GLP-1 peptides that also blocks the GIP receptor. In plain terms: it combines appetite signals in one long-lasting molecule you inject only once a month. It is still experimental.
NA-931, also called Bioglutide, is an experimental obesity compound from Biomed Industries of San Jose. The company describes it as a first-in-class quadruple receptor agonist acting at the IGF-1, GLP-1, GIP and glucagon receptors, given as a once-daily capsule. It is the compound behind the 'GLP-4' label that sellers have put on injectable vials, a description that fits neither the capsule nor the company.
Pemvidutide is a dual GLP-1 and glucagon agonist. In plain terms: it curbs appetite and nudges metabolism to burn more, studied for both weight loss and fatty-liver disease. It is still experimental.
VK2735 is a dual GLP-1 and GIP agonist, the same two-receptor family as tirzepatide. In plain terms: it works on two appetite-and-blood-sugar signals for weight loss, with promising early results. It is in trials as both a shot and a pill.
Zovaglutide is a long-acting GLP-1 receptor agonist. In plain terms: it gives the usual GLP-1 appetite control but lasts long enough to inject just once a month. It is still experimental.
Amylin analogs
Copies of amylin, the fullness hormone your pancreas releases alongside insulin.
Cagrilintide is a long-acting amylin analog, a copy of amylin, the hormone your pancreas releases with insulin to signal fullness. In plain terms: it works on a different 'stop eating' pathway than the GLP-1 drugs, which is why it is often paired with semaglutide for bigger results.
Eloralintide is an amylin receptor agonist from Eli Lilly. In plain terms: it copies the pancreas's fullness hormone for weight loss, designed to be easy to tolerate. It is still in trials.
Petrelintide is a long-acting amylin analog. In plain terms: it copies the pancreas's fullness hormone to reduce appetite, positioned as a gentler standalone weight-loss option. It is still experimental.
Pramlintide is a synthetic version of amylin, a hormone released with insulin. In plain terms: taken at meals alongside insulin in diabetes, it blunts the post-meal blood-sugar spike and reduces hunger. It is FDA-approved.
Fat loss without GLP-1
The weight-loss compounds that are not GLP-1 or amylin drugs. People arrive here looking for something that works like Ozempic without being Ozempic.
5-Amino-1MQ is a small molecule, not a peptide, that blocks an enzyme called NNMT which helps fat cells store fat. In plain terms: by taking the brakes off cellular metabolism, it is studied for burning fat and boosting energy, though human data is very limited.
AOD-9604 is a modified fragment of growth hormone (the 176-191 tail) with an added amino acid. In plain terms: it was built to trigger growth hormone's fat-burning effect without its muscle or blood-sugar effects, though the human proof that it works is weak.
Melanotan II is a broad melanocortin-receptor agonist, hitting several of the same receptors as the tanning and libido hormones. In plain terms: it tans skin fast and also boosts libido and cuts appetite, but hitting so many receptors is why it has more side effects. It is not approved.
SLU-PP-332 is a small molecule, not a peptide, that activates ERR, a switch controlling how cells burn energy. In plain terms: it is nicknamed 'exercise in a molecule' because it pushes cells to act as if you had worked out, but it is very early with no human data.
GHRP-6 is a growth hormone releasing peptide that strongly activates the ghrelin (hunger) receptor. In plain terms: it raises your own growth hormone and triggers intense hunger, which is why it is mostly used for bulking.
Levocarnitine is a naturally occurring compound that carries long-chain fatty acids across the mitochondrial membrane so they can be burned for energy. In plain terms: it is the shuttle that moves fat into the part of the cell that burns it.
HGH Fragment 176-191 is the tail end of the growth hormone molecule, the part linked to fat breakdown. In plain terms: it aims to target stubborn fat without the rest of growth hormone's effects, but real human evidence is thin.
Tesofensine is a small molecule, not a peptide, that blocks the reuptake of three brain chemicals: dopamine, noradrenaline, and serotonin. In plain terms: it acts on the brain's appetite and reward system like a stimulant to suppress hunger, which also means more heart-related risk.
Adipotide is an experimental peptide that homes to the blood vessels feeding fat tissue and triggers them to die. In plain terms: by starving fat of its blood supply it caused dramatic fat loss in animals, but it also damaged kidneys, so it is considered dangerous with essentially no safe human use.
AICAR is a small molecule that switches on AMPK, the enzyme cells use to sense low energy. In plain terms: it produces some of the changes exercise produces, and the amounts used in the famous animal studies do not scale to a person.
Humanin is a mitochondrial-derived peptide, a short chain encoded inside your mitochondria's own DNA. In plain terms: it acts as a cell-protective, stress-resistance signal, which is why it is studied for brain, metabolic, and aging support. Human data is limited.
BAM15 is a small molecule, not a peptide. It makes your mitochondria waste energy on purpose. Mitochondria normally build up a charge and then use it to make cellular fuel. BAM15 lets that charge leak away as heat instead, so the cell has to burn more to keep up. In plain terms: it turns your cells into slightly less efficient engines, so they burn more for the same work. It has never been tested in a person.
Pancragen is a 4-amino-acid 'bioregulator' from the Russian Khavinson family. In plain terms: it is marketed for pancreas function and blood sugar with age, but there is very little real human research behind it.
Lipo-C is a compounded sterile injection of lipotropic agents, most often methionine, inositol and choline, usually with vitamin B12 and sometimes L-carnitine, in a multi-dose vial. In plain terms: it is a vitamin and amino acid shot given weekly at clinics and sold as a fat-loss aid.
GW501516 is a PPAR-delta agonist developed as a metabolic drug and abandoned. In plain terms: animal testing found tumours across multiple organs, development stopped, and it is still sold as an endurance supplement.
ATX-304 is a first-in-class pan-AMPK activator that works by protecting the Thr172 site from dephosphorylation, keeping AMPK switched on without lowering cellular ATP. In plain terms: it holds down the switch the body normally flips during exercise or fasting.
SR9009 is a small molecule that acts on REV-ERB, part of the machinery running the body clock. In plain terms: it is sold as exercise in a capsule, and published work found it is barely absorbed when swallowed.
Adropin is a peptide the body makes, studied mostly as a blood marker linked to insulin sensitivity and fatty liver. In plain terms: most of what is known about it comes from measuring it, not from giving it to anyone.
Irisin is a fragment released from a muscle protein during exercise, reported to turn white fat into calorie-burning brown fat. In plain terms: it made headlines as exercise in a molecule, and the tools used to measure it in blood were then shown to be unreliable.
Setmelanotide is an MC4R agonist that switches on the brain's melanocortin-4 receptor, a master control for hunger. In plain terms: for people with rare genetic defects in this exact hunger pathway, it restores the missing 'I'm full' signal. It is FDA-approved only for those specific conditions.
Spexin is a short peptide identified by searching genome databases rather than by isolating it from tissue. In plain terms: animal work links it to appetite and body weight, and there is no human trial of giving it.
Weekly dual-receptor CT-388 and monthly GLP-1 zovaglutide have not been compared head to head; their trial results use different measures and follow-up periods.
In STEP 8, semaglutide produced more weight loss than liraglutide; liraglutide offers generic availability and daily dosing.
One receptor, then two, then three, and the numbers climb with them. Only two of the three steps have a head to head behind them.
Both were tested in the same trial, in the same people, over the same 68 weeks. Semaglutide won on weight, and the combination beat both while coming in below their sum.
Tirzepatide won the head-to-head at 20.2 percent against 13.7. The 47 percent figure everyone quotes is relative; the absolute gap is 6.5 points, from an open-label trial.
Retatrutide's 28.3 percent is being set against tirzepatide's 22.5 percent. Different trials, different lengths, and one of the numbers comes from a press release.
Common questions
What is the best peptide for weight loss?
The strongest evidence belongs to the GLP-1 drugs. Semaglutide and tirzepatide both have approved weight-loss products in the United States and large published trials, and in a head-to-head trial tirzepatide produced more weight loss than semaglutide. Tirzepatide also acts on a second gut-hormone receptor, GIP.
Are there weight-loss peptides that are not GLP-1 drugs?
Yes. Amylin analogs such as cagrilintide act on a separate fullness hormone and have human trial results, both alone and paired with semaglutide. Beyond those, the evidence for ordinary weight loss drops off sharply. AOD-9604 went through human trials and did not meet its primary endpoint, and most of the rest have never been tested for weight loss in a person.
Do you need a prescription for weight-loss peptides?
In the United States the approved GLP-1 weight-loss products are prescription drugs. Most other compounds on this page are not approved for any use and are sold as research chemicals rather than medicines. Each compound page lists its own status.
