Weight Loss Peptides

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GLP-1 receptor agonists like Semaglutide and Tirzepatide have transformed obesity research, with newer triple agonists like Retatrutide showing even greater potential. This category covers every peptide studied for appetite regulation, fat metabolism, and weight management — from FDA-approved medications to experimental compounds.

5-Amino-1MQ

Weight LossMetabolic

A pill that aims to switch fat cells from 'storage mode' to 'burning mode' by blocking an enzyme (NNMT) that is overactive in the fat tissue of overweight people. Not technically a peptide, but commonly sold alongside them. Unlike appetite suppressants, this targets the fat cells directly rather than making you eat less. The science is promising in lab studies, but there are no completed human trials yet.

Fat MetabolismMetabolic EnhancementInsulin Sensitivity
Half-life:12-16 hours (limited pharmacokinetic data)

Adipotide

Weight Loss

An extreme experimental approach to fat loss — it physically destroys the blood vessels that feed fat tissue, starving fat cells until they die. Originally developed using anti-cancer technology at MD Anderson Cancer Center. While it did reduce fat in monkey studies, it also caused serious kidney damage, which has effectively stopped its development. Not available for human use.

Fat DestructionWeight Loss
Half-life:Estimated 2-4 hours (limited pharmacokinetic data)

Amycretin

Weight Loss

Novo Nordisk's next-generation weight loss drug — the first single molecule that combines two appetite hormones (GLP-1 and amylin) in one shot. The same effect that CagriSema needs two drugs to achieve, amycretin does on its own. In Phase 1b/2a trials, people lost up to 22% of their body weight in 36 weeks, and a once-daily oral pill version is being developed alongside the weekly injection. Phase 3 trials began in 2026. Also known as zenagamtide.

Weight LossAppetite SuppressionGlycemic ControlOral Bioavailability
Half-life:Approximately 168 hours (7 days) for the subcutaneous formulation

AOD-9604

Weight Loss

A small piece of human growth hormone (amino acids 176-191) designed to keep only the fat-burning effects while removing the unwanted side effects of full growth hormone (like swelling and blood sugar problems). The idea is promising — burn fat without the downsides — but it failed to show significant weight loss in clinical trials. Still widely used in research and wellness clinics despite the weak clinical evidence.

Fat MetabolismLipogenesis InhibitionIGF-1 Neutral
Half-life:1-2 hours

AT7687

Weight LossMetabolic

A novel obesity drug from Danish biotech Antag Therapeutics that takes a completely different approach — instead of suppressing appetite like all the GLP-1 drugs, it stops fat from being stored in the first place by blocking the GIP receptor in fat cells. First-in-human Phase 1 trial completed in 2026 showed it is well tolerated, with mild GI side effects, and produced reductions in LDL cholesterol and resting heart rate alongside weight loss signals.

Fat Storage BlockadeLipid ProfileCardiovascularGI Tolerability
Half-life:Approximately 7-10 days, supporting once-weekly dosing

Cagrilintide

Weight Loss

A long-acting version of amylin, a natural hormone your body releases after eating that tells your brain you're full. It works through a completely different pathway than GLP-1 drugs like semaglutide, which is why combining them (as CagriSema) produces even better results. On its own, it reduces how much you eat per meal by signalling fullness earlier. Developed by Novo Nordisk, mainly as part of the CagriSema combination.

Appetite SuppressionWeight LossSatiety Enhancement
Half-life:168 hours (7 days)

CagriSema

Weight Loss

A once-weekly injection that combines two powerful appetite-suppressing drugs — cagrilintide and semaglutide — into a single shot. By targeting two different hunger pathways in the brain simultaneously, it achieves roughly 25% body weight loss in trials, making it one of the most effective weight loss treatments ever developed. Think of it as the next generation beyond Wegovy. Still awaiting FDA approval.

Weight LossAppetite SuppressionBlood Sugar Control
Half-life:168 hours (7 days) for both components

CT-388

Weight Loss

Roche's once-weekly weight loss injection that targets the same two appetite hormones as tirzepatide (GLP-1 and GIP). Originally developed by Carmot Therapeutics before Roche acquired the company in 2024 specifically to obtain this molecule. In a Phase 2 trial of 469 people, it produced up to 22.5% placebo-adjusted body weight loss at 48 weeks — competitive with tirzepatide and showing no sign of plateau at the highest dose. Phase 3 trials started in 2026.

Weight LossAppetite SuppressionGlycemic ControlGI Tolerability
Half-life:Approximately 168 hours (7 days), supporting once-weekly dosing

Danuglipron

Weight LossMetabolic

Pfizer's once-failed attempt at an oral GLP-1 weight loss pill (code name PF-06882961). Despite producing meaningful weight loss in Phase 2 trials, Pfizer discontinued development in 2025 after reports of potential liver injury in a healthy volunteer. Included here because it remains heavily searched as the cautionary tale of the oral GLP-1 race — and because Pfizer is now developing alternative oral GLP-1 candidates after the danuglipron setback.

Weight LossGlycemic ControlOral BioavailabilityGI Tolerability
Half-life:Approximately 6-9 hours, designed for twice-daily oral dosing

Ecnoglutide

Weight LossMetabolic

A long-acting weekly GLP-1 weight loss injection from Chinese biotech Sciwind Biosciences. Uses a special protein-extension technology to last longer in the body than semaglutide. Late-stage Phase 3 trials in China showed body weight loss of 14-15% in obesity and good blood-sugar control in type 2 diabetes. Approval in China is expected first, with international filings to follow. One of several Chinese-developed GLP-1s reaching the global market.

Weight LossGlycemic ControlAppetite SuppressionOnce-Weekly Dosing
Half-life:Approximately 7-10 days, supporting once-weekly dosing

GLP-1

Weight LossMetabolic

The natural appetite hormone that your gut produces after eating — it's what all GLP-1 weight loss drugs (semaglutide, tirzepatide, etc.) are designed to copy. Your body makes it naturally, but it breaks down within 1-2 minutes, which is far too fast to use as a medicine. That's why drug companies created modified versions that last days instead of minutes. Included here because understanding GLP-1 is key to understanding the entire class of modern weight loss drugs.

Blood Sugar ControlAppetite SuppressionGastric Emptying
Half-life:1-2 minutes

HGH Fragment 176-191

Weight Loss

The original, unmodified version of the growth hormone fat-burning fragment — essentially the same concept as AOD-9604 but less stable and shorter-lasting. Contains the part of growth hormone responsible for fat metabolism without the parts that cause growth or blood sugar issues. Requires more frequent dosing than AOD-9604, and has even less clinical evidence supporting its effectiveness.

Fat MetabolismIGF-1 NeutralWeight Loss
Half-life:0.5-1 hours

L-Carnitine

Weight LossMetabolic

A natural substance your body already makes that acts as a 'shuttle' to carry fat into your cells' energy factories (mitochondria) where it gets burned for fuel. Without enough carnitine, your body literally cannot burn long-chain fats for energy. One of the most popular and well-studied fat metabolism supplements available. Has FDA-approved forms for people with carnitine deficiency, and is widely available over the counter as a supplement.

Fat TransportExercise PerformanceMetabolic Support
Half-life:2-3 hours (injectable); oral bioavailability 15-25%

Lemon Bottle

BeautyWeight Loss

A cosmetic fat-dissolving injection from South Korea that is injected directly into stubborn fat areas (like a double chin or love handles) to break down fat cells locally. Contains vitamin B2, lecithin (a natural fat emulsifier), and bromelain (a pineapple enzyme). This is not a weight loss treatment — it's a targeted body contouring procedure, similar to CoolSculpting but using injections instead of cold. Requires multiple sessions.

Localized Fat ReductionCosmetic ContouringSkin Tightening
Half-life:Components metabolized within hours; visible effects develop over 2-4 weeks

Lipo-C

Weight LossMetabolic

A vitamin and amino acid injection commonly offered at weight loss clinics to support fat metabolism. Contains a mix of nutrients (methionine, inositol, choline, B vitamins, and L-carnitine) that help your liver process and export fat, and help your cells burn fat for energy. Think of it as a metabolic support shot — it's not a standalone weight loss treatment, but is used alongside diet and exercise to help your body process fat more efficiently.

Hepatic Fat ProcessingFat Oxidation SupportMetabolic Support
Half-life:Variable by component; effects are cumulative with regular dosing

Liraglutide

Weight LossMetabolic

A GLP-1 medication that mimics a natural gut hormone (97% similar to native GLP-1) and is the predecessor to semaglutide. FDA-approved for both type 2 diabetes (Victoza) and obesity (Saxenda). One of the most prescribed weight loss medications worldwide, with extensive long-term safety data including reduced risk of heart attack and stroke in diabetic patients.

Weight LossBlood Sugar ControlCardiovascular Protection
Half-life:13 hours

MariTide

Weight Loss

Amgen's monthly weight loss injection — and the only one in late-stage development you only have to take every four weeks rather than every week. Unusually, it activates GLP-1 but blocks GIP (most other dual drugs activate both). In Phase 2 it produced around 20% body weight loss at 52 weeks, with the added benefit of slow weight regain after stopping treatment in animal studies. Phase 3 MARITIME trials started in 2026. Generic name maridebart cafraglutide.

Weight LossMonthly DosingSlow Weight RegainNovel Mechanism
Half-life:Approximately 21 days, supporting once-monthly dosing

Mazdutide

Weight Loss

A weight loss injection that suppresses appetite while also boosting your metabolism and helping your liver burn fat. Approved in China for obesity in 2024, with up to 14% body weight loss in trials. It targets two hormones — GLP-1 (which reduces hunger) and glucagon (which increases calorie burning and liver fat breakdown). Particularly promising for people with fatty liver disease alongside obesity.

Weight LossLiver Fat ReductionBlood Sugar Control
Half-life:144-192 hours (6-8 days)

NN1706

Weight Loss

Novo Nordisk's answer to retatrutide — a once-daily injection that activates all three of the major appetite and metabolism hormones (GLP-1, GIP, and glucagon). The first human data was published in 2026, showing meaningful weight loss in obese subjects and confirming the daily-dosing mechanism is tolerable. Direct competitor to Lilly's once-weekly retatrutide, with the trade-off of more frequent dosing in exchange for potentially smoother side-effect control and easier dose adjustment.

Weight LossEnergy ExpenditureGlycemic ControlDaily Dosing
Half-life:Approximately 14-18 hours, supporting once-daily dosing

Orforglipron

Weight LossMetabolic

The first weight loss drug in the GLP-1 class that comes as a daily pill rather than a weekly injection — and unlike Rybelsus, you can take it with food and water. Made by Eli Lilly, it is technically a small molecule rather than a peptide, but it activates the same GLP-1 receptor as semaglutide and tirzepatide. Phase 3 trials in 2026 (ACHIEVE-1 in diabetes, ATTAIN-1 and ATTAIN-2 in obesity) have shown around 14-15% body weight loss. Likely to be the first oral GLP-1 to compete on weight loss with the injectables.

Weight LossOral BioavailabilityGlycemic ControlOnce-Daily Dosing
Half-life:Approximately 29-49 hours, supporting once-daily oral dosing

Pemvidutide

Weight LossMetabolic

A weekly weight loss injection from Altimmune that targets two hormones (GLP-1 for appetite, glucagon for fat-burning) — similar to mazdutide and survodutide. Particularly being developed for fatty liver disease (MASH) alongside obesity. Phase 2b results showed around 15.6% body weight loss at 48 weeks, with significant reductions in liver fat. Also branded as ALT-801. Now in Phase 3 trials for both indications.

Weight LossLiver Fat ReductionEnergy ExpenditureAppetite Suppression
Half-life:Approximately 168 hours (7 days), supporting once-weekly dosing

Retatrutide

Weight Loss

The first weight loss drug to target three appetite and metabolism hormones at once (GIP, GLP-1, and glucagon). In early trials, people lost up to 24% of their body weight — the highest ever recorded for any weight loss medication. The third hormone target (glucagon) helps burn more calories and reduce liver fat, going beyond what current drugs like semaglutide or tirzepatide can achieve. Still in clinical trials.

Weight LossEnergy ExpenditureLiver Fat ReductionBlood Sugar Control
Half-life:144 hours (6 days)

Semaglutide

Weight Loss

The most widely prescribed weight loss medication in the world, sold as Wegovy and Ozempic. Works by dramatically reducing appetite and food cravings — most people report feeling full much faster and losing interest in snacking. In clinical trials, patients lost an average of 15-17% of their body weight. Also available as a daily pill (Rybelsus). Originally developed for type 2 diabetes, it also helps control blood sugar levels.

Weight LossAppetite SuppressionBlood Sugar ControlGastric EmptyingCardiovascular Benefit
Half-life:168 hours (7 days)

Survodutide

Weight Loss

A weight loss injection being developed specifically for both obesity and fatty liver disease (MASH). It reduces appetite through one pathway while simultaneously telling your liver to burn its stored fat through another. This dual approach tackles the root cause (eating too much) and the downstream damage (fat build-up in the liver) at the same time. Still in clinical trials.

Liver Fat ReductionWeight LossEnergy Expenditure
Half-life:144 hours (6 days)

Tesamorelin

Weight LossBodybuilding

The only growth hormone peptide with active FDA approval — sold as Egrifta for reducing dangerous belly fat (visceral fat) in HIV patients. It's especially effective at targeting the deep fat around your organs, which is the most harmful type. Widely used off-label by people wanting to improve body composition, reduce belly fat, and address fatty liver. In trials it reduced trunk fat by 15-18%.

Visceral Fat ReductionGH ReleaseLiver Health
Half-life:26-38 minutes

Tesamorelin + Ipamorelin

BodybuildingAnti-AgingWeight Loss

A popular combination pairing Tesamorelin (FDA-approved for certain conditions) with Ipamorelin to boost growth hormone. Favored for improving body composition, reducing belly fat, and anti-aging. Tesamorelin has proven effectiveness for visceral fat reduction, and Ipamorelin has a clean side-effect profile, making this a premium GH peptide protocol.

Visceral Fat TargetingBody Composition
Half-life:Tesamorelin: 26 minutes | Ipamorelin: 2 hours

Tesofensine

Weight Loss

A medication that blocks reuptake of serotonin, dopamine, and norepinephrine — originally developed for Alzheimer's and Parkinson's but showed significant weight loss in clinical trials. Reduces appetite through brain signaling in appetite centers. A different approach than GLP-1 medications and other peptide-based weight loss treatments.

Weight LossAppetite SuppressionEnergy Expenditure
Half-life:192-216 hours (8-9 days)

Tirzepatide

Weight Loss

Sold as Mounjaro and Zepbound, this is one of the most effective weight loss medications available. It works by targeting two appetite hormones at once (GIP and GLP-1), making it more powerful than medications like semaglutide that only target one. People in clinical trials lost up to 22.5% of their body weight. Also FDA-approved for type 2 diabetes, and improves cholesterol and blood fat levels.

Weight LossAppetite SuppressionBlood Sugar ControlLipid Improvement
Half-life:120 hours (5 days)

VK2735

Weight Loss

Viking Therapeutics' once-weekly weight loss injection that, like tirzepatide, hits both the GLP-1 and GIP receptors. In a 13-week Phase 2 trial it produced 14.7% mean body weight loss — the steepest early loss curve recorded for any obesity drug — and Phase 3 VANQUISH trials began in 2026. An oral tablet version is also in earlier development. Viking is one of the only small biotech companies competing directly with Lilly and Novo Nordisk in the GLP-1 space.

Weight LossAppetite SuppressionGlycemic ControlOral Formulation
Half-life:Approximately 144-168 hours (6-7 days), supporting once-weekly dosing