Category · 30 entries

Metabolic & Weight Loss

GLP-1 agonists and related metabolic peptides.

Discontinued

Albiglutide

An FDA- and EMA-approved once-weekly GLP-1 agonist (Tanzeum / Eperzan, GSK) withdrawn from the market in 2018 for commercial rather than safety reasons after failing to differentiate commercially against dulaglutide and semaglutide.

Research Only

AOD-9604

A short GH fragment marketed heavily as a "fat-loss peptide" — but with a clinical record that has not supported meaningful weight loss in humans.

Not Approved (US)

Beinaglutide

A recombinant native-sequence GLP-1 peptide approved in China (NMPA 2016) for type 2 diabetes and 2023 for obesity — notable as the only marketed GLP-1 RA with the native, unmodified human GLP-1(7-36) sequence, requiring three-times-daily dosing because of its short half-life.

Clinical Trials

Cagrilintide

A once-weekly amylin analog developed primarily as a combination partner for semaglutide (CagriSema), adding amylin-pathway appetite suppression to GLP-1 activity.

FDA Approved

Dulaglutide

A weekly GLP-1 agonist for type 2 diabetes, delivered as a GLP-1/IgG4 fusion protein in a single-use auto-injector.

Not Approved (US)

Ecnoglutide

Sciwind Biosciences' GLP-1 agonist — approved in China (NMPA, March 2026) for obesity and type 2 diabetes; not FDA-approved. Distinguished from other GLP-1s by "biased agonism" selectively activating cAMP over β-arrestin recruitment.

FDA Approved

Exenatide

The first GLP-1 receptor agonist to reach market (2005), available in both twice-daily and weekly extended-release formulations.

FDA Approved

Glucagon

The endogenous counter-regulatory hormone to insulin — FDA-approved for severe hypoglycemia (injectable GlucaGen, nasal Baqsimi, autoinjector Gvoke). Also the pharmacological template for GLP-1/glucagon dual agonists like Pemvidutide and Retatrutide.

FDA Approved

Insulin aspart

Novo Nordisk's rapid-acting insulin analog (NovoLog / NovoRapid, approved 2000) — the B28 proline → aspartate substitution destabilizes hexamer formation, and the ultra-rapid Fiasp formulation (2017) adds niacinamide and L-arginine for even faster absorption.

FDA Approved

Insulin degludec

Novo Nordisk's ultra-long-acting insulin (Tresiba, 2015) — forms soluble multi-hexamers in SC tissue that slowly dissociate for a >42-hour half-life and a flat, forgiving dosing window; the basal insulin with the lowest hypoglycemia risk profile.

FDA Approved

Insulin degludec / liraglutide (IDegLira)

Novo Nordisk's fixed-ratio insulin/GLP-1 combo pen (Xultophy, FDA 2016) — 100 units/mL insulin degludec + 3.6 mg/mL liraglutide; simplifies T2DM therapy intensification into a single daily injection with additive glycemic benefit and less weight gain than basal insulin alone.

Discontinued

Insulin detemir

Novo Nordisk's fatty-acid-acylated basal insulin (Levemir, 2005) — the myristoyl chain enables reversible albumin binding, extending the half-life; Novo Nordisk announced global discontinuation in December 2023 (US supply ended 2024).

FDA Approved

Insulin glargine

The dominant once-daily basal insulin for two decades (Lantus, Sanofi, 2000) — the pI-shift design causes microprecipitation in subcutaneous tissue for a nearly peakless 24-hour absorption profile; Toujeo (U-300) is the same molecule at 3× concentration.

FDA Approved

Insulin glargine / lixisenatide (iGlarLixi)

Sanofi's fixed-ratio insulin/GLP-1 combo pen (Soliqua, FDA 2016) — 100 units/mL insulin glargine + 33 mcg/mL lixisenatide; a parallel to Xultophy, differentiated by using short-acting prandial-biased lixisenatide rather than liraglutide.

FDA Approved

Insulin glulisine

Sanofi's rapid-acting insulin analog (Apidra, 2004) — the third rapid-acting analog approved, differentiated by being zinc-free in formulation, which gives it slightly faster monomeric onset than lispro or aspart.

Not Approved (US)

Insulin icodec

Novo Nordisk's once-weekly basal insulin (Awiqli, EMA 2024) — the first weekly insulin to reach market; FDA refused to approve in July 2024 (CRL citing type 1 diabetes hypoglycemia data), leaving it approved in the EU, UK, Canada, Switzerland, and Japan while pending US resubmission.

FDA Approved

Insulin lispro

The first FDA-approved rapid-acting insulin analog (Humalog, Lilly, 1996) — the B28–B29 position swap prevents hexamer self-association, producing faster subcutaneous absorption than regular human insulin.

FDA ApprovedFull Entry

Liraglutide

The first once-daily GLP-1 analog to be FDA-approved for both type 2 diabetes (Victoza) and chronic weight management (Saxenda).

FDA Approved

Lixisenatide

A short-acting, prandial GLP-1 agonist primarily used to target postprandial glucose excursions.

In Development

Mazdutide

A weekly GLP-1/glucagon dual agonist approved in China for obesity (2025); the first OXM-mimetic to reach market.

FDA Approved

NPH insulin (isophane)

The classical intermediate-acting insulin — regular human insulin co-crystallized with protamine to produce ~12-hour action; still widely used for cost reasons despite being largely superseded by analog basal insulins for T1DM.

Clinical Trials

Orforglipron

⚠ Not a peptide — small molecule. A daily oral GLP-1 agonist in Phase 3 for obesity and T2DM, distinct from Rybelsus in being a small molecule rather than an oral peptide formulation. Included in this peptide encyclopedia because the audience frequently searches for it alongside peptide GLP-1 agonists.

FDA Approved

Pramlintide

The FDA-approved amylin analog (Symlin, 2005) — taken at mealtimes alongside insulin in T1D and T2D. The pharmacological proof-of-concept for amylin agonism that petrelintide and cagrilintide are now building on.

FDA Approved

Regular human insulin

The original recombinant human insulin (Humulin R, 1982) — unmodified native sequence, short-acting kinetics driven by hexamer self-association; U-500 concentration for severely insulin-resistant patients.

Clinical TrialsFull Entry

Retatrutide

An investigational triple hormone agonist that produced ~24% weight loss at 48 weeks in Phase 2 — the largest in any single-agent obesity trial to date.

FDA ApprovedFull Entry

Semaglutide

A once-weekly GLP-1 receptor agonist FDA-approved for type 2 diabetes and chronic weight management.

FDA Approved

Setmelanotide

Rhythm Pharmaceuticals' Imcivree — the first and only FDA-approved MC4R agonist. Indicated for obesity due to POMC, PCSK1, or LEPR deficiency (2020) and Bardet-Biedl syndrome (2022). Restores downstream MC4R signaling when upstream leptin-melanocortin pathway components are genetically deficient.

Clinical Trials

Survodutide

A once-weekly GLP-1/glucagon co-agonist in late-stage trials for obesity, type 2 diabetes, and MASH.

FDA Approved

Teduglutide

FDA-approved GLP-2 analog (Gattex/Revestive, 2012) for short-bowel syndrome — the first disease-modifying treatment for SBS, reducing parenteral nutrition dependence by promoting intestinal mucosal growth.

FDA ApprovedFull Entry

Tirzepatide

A once-weekly GLP-1/GIP dual agonist that produced unprecedented weight loss in SURMOUNT trials — up to ~21% at highest dose.

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