| SemaglutideWegovy, Ozempic, Rybelsus | Prescribed as Wegovy for weight management; compounded semaglutide is a separate preparation.FDA-approved for this | The Wegovy label carries a full weekly schedule, from a 0.25 mg starting dose up to 1.7 mg or 2.4 mg. Ozempic and Rybelsus are separate semaglutide products with different approved uses. | FDA labelDose from the FDA-approved label |
|---|
| TirzepatideZepbound, Mounjaro | Prescribed as Zepbound for weight management; also sought as compounded tirzepatide.FDA-approved for this | The Zepbound label starts at 2.5 mg once weekly for four weeks. This is a starting dose, not a maintenance dose. Later increases are in 2.5 mg steps after at least four weeks at the current dose. | FDA labelDose from the FDA-approved label |
|---|
| LiraglutideVictoza, Saxenda | Prescribed as Saxenda for chronic weight management, while the same molecule is also sold as the separate diabetes product Victoza.FDA-approved for this | Saxenda starts at 0.6 mg once daily and steps weekly to 3 mg daily. Victoza has a different use and stops lower. Keep the product name with the schedule. | FDA labelDose from FDA-approved product labels |
|---|
| Retatrutide | Sought for weight loss while it remains an experimental drug.Being tested for this in trials | Its 48-week phase 2 trial ran 1, 4, 8 and 12 mg weekly arms, reached by stepping up. The 12 mg arm produced the largest weight change in the program. It has no approved label and no approved dose. | Human trialDose from a human trial · no FDA label |
|---|
| Survodutide | Studied as an experimental treatment for weight loss.Being tested for this in trials | Over 46 weeks, weekly doses of 0.6 to 4.8 mg produced mean weight change of −6.2% to −14.9%, against −2.8% on placebo. It is in phase 3. The trial schedule is not an approved prescribing schedule. | Human trialDose from a human trial · no FDA label |
|---|
| Cagrilintide | Studied for weight loss alone and in combination with semaglutide.Being tested for this in trials | Its phase 2 trial ran weekly doses from 0.3 mg to 4.5 mg. The 2.4 mg dose went into phase 3 together with semaglutide 2.4 mg. The pairing people copy is a formulated product, not two vials mixed at home. | Human trialDose from a human trial · no FDA label |
|---|
| Mazdutide | Prescribed as Xinermei for weight management in China and sought in the United States as a newer GLP-1/glucagon trial drug.Approved outside the U.S. | China approved mazdutide for weight in 2025; FDA has not. A 48-week trial reported mean changes of −11.0% and −14.01% for 4 mg and 6 mg, versus +0.3% with placebo. | Human trialDose from a human trial · no FDA label |
|---|
| VK2735 | Sought as an experimental weekly injection or separate tablet while its phase 3 weight-management program is still running.Being tested for this in trials | A 13-week phase 2 injection trial reported average weight changes from −9.1% to −14.7% across four dose groups, versus −1.7% with placebo. The phase 3 trials have no results yet. | Human trialDose from a human trial · no FDA label |
|---|
| Zenagamtide | Followed under its current name and its former name, Amycretin, as an experimental injection and oral weight-loss program.Being tested for this in trials | An early injection trial reported 24.3% average weight loss in the 60 mg group at week 36, versus 1.1% with placebo. Its registered phase 3 studies have no results yet. | Human trialDose from a human trial · no FDA label |
|---|
| Pemvidutide | Sought as an experimental weekly GLP-1/glucagon injection on the strength of its obesity and liver-disease programs.Being tested for this in trials | The sponsor reported average weight changes from −10.3% to −15.6% across three groups at week 48, versus −2.2% with placebo. Pemvidutide is not FDA-approved. | Human trialDose from a human trial · no FDA label |
|---|
| TesamorelinEgrifta SV, Egrifta WR | Sought for belly fat beyond the specific HIV-related condition covered by its approval.Measured in a human study | Its approved use is excess abdominal fat in adults with HIV-related lipodystrophy. The label says it is not a weight-loss treatment and describes its effect on body weight as neutral. | FDA labelDose from the FDA-approved label |
|---|
| AOD-9604 | Sold for fat loss, on the idea that this fragment of growth hormone carries the fat-mobilizing part alone.Measured in a human study | The larger controlled obesity trials did not show a benefit over placebo. An Australian company ran controlled human obesity trials; the larger ones did not separate it from placebo, and development stopped. The 10 mg group lost less than the 1 mg group. Every trial dose was swallowed, not injected, and the primary trial reports were never published. | limited human dataDose reported in the literature only |
|---|
| MOTS-c | Sold for fat loss and metabolic aging, on the observation that natural blood levels fall as people get older.Reported use only | The cited metabolic experiments used mice. Human observations linked natural levels with age, but did not test whether giving MOTS-c causes weight loss. No human weight-loss dose is established in these sources. | no human dose shown to workNo human dose published |
|---|
| Ipamorelin | Offered for fat loss based on its growth-hormone effect.Reported use only | Its two completed trials tested how quickly the gut restarted after bowel surgery, and neither beat placebo. No trial has measured fat. The growth-hormone pulse it produces is real and measured; these sources do not show that it causes fat loss. | Human trialDose from a human trial · no FDA label |
|---|
| CJC-1295 | Sold for fat loss, often paired with ipamorelin.Reported use only | The cited human studies measured growth hormone and IGF-I in the blood. They did not report weight loss or changes in body fat. They studied the long-acting form with a drug-affinity complex; products labeled without DAC are a different form. | limited human dataDose from a human trial · no FDA label |
|---|