The main GLP-1 receptor agonist (GLP-1 RA) brands, grouped by active ingredient, are:
Active Ingredient | Key Brand Names | Manufacturer | Primary Indications |
|---|---|---|---|
Semaglutide | Ozempic (weekly injection) Rybelsus (daily oral tablet) Wegovy (weekly injection, higher dose) | Novo Nordisk | Type 2 diabetes (Ozempic, Rybelsus); chronic weight management (Wegovy) |
Liraglutide | Victoza (daily injection) Saxenda (daily injection, higher dose) | Novo Nordisk | Type 2 diabetes (Victoza); chronic weight management (Saxenda) |
Dulaglutide | Trulicity (weekly injection) | Eli Lilly | Type 2 diabetes; cardiovascular risk reduction |
Tirzepatide (dual GIP/GLP-1 RA) | Mounjaro (weekly injection) Zepbound (weekly injection, higher dose) | Eli Lilly | Type 2 diabetes (Mounjaro); chronic weight management (Zepbound) |
Exenatide | Byetta (twice-daily injection) Bydureon / Bydureon BCise (weekly injection) | AstraZeneca | Type 2 diabetes |
Lixisenatide | Adlyxin (daily injection) | Sanofi | Type 2 diabetes |
Albiglutide (discontinued 2017) | Tanzeum | GSK | — |
Notes
- Semaglutide and tirzepatide dominate current prescriptions due to superior A1C reduction and weight-loss data.
- All except Rybelsus are injectable; Rybelsus is the only oral GLP-1.
GLP-1 drugs (GLP-1 receptor agonists, or GLP-1 RAs) mimic the action of the natural hormone GLP-1 (glucagon-like peptide-1), which is released by intestinal L-cells after eating. They bind to and activate GLP-1 receptors on various tissues, producing coordinated effects that lower blood glucose and promote weight loss.
Core Mechanisms of Action
Effect | How It Works | Clinical Outcome |
|---|---|---|
↑ Insulin secretion (glucose-dependent) | Stimulates pancreatic β-cells to release insulin only when blood glucose is high. | Lowers post-meal blood sugar spikes; minimal hypoglycemia risk. |
↓ Glucagon secretion | Suppresses α-cells in the pancreas from releasing glucagon (especially when glucose is high). | Reduces liver glucose production. |
↓ Gastric emptying | Slows the rate at which food leaves the stomach. | Prolongs satiety; blunts post-meal glucose peaks. |
↑ Satiety (appetite suppression) | Acts on GLP-1 receptors in the hypothalamus (brain). | Reduces hunger and calorie intake → weight loss. |
↓ Hepatic glucose output | Indirectly via reduced glucagon and improved insulin sensitivity. | Lowers fasting blood glucose. |
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