WIKI · MAINTAINED BY THE MOD TEAM · UPDATED JUN 2026
Welcome to The GLP Lounge. This guide is the community's front door: a plain-English orientation to GLP-1 receptor agonists — semaglutide, tirzepatide, retatrutide and friends — plus the practical things every newcomer asks in their first week.
Visual summary of STEP, SURMOUNT, TRIUMPH and the cardiovascular outcome trials.
Reconstitution math with a visual syringe — mg, mL, and insulin units.
Real incidence data and evidence-based management for GI effects and beyond.
How to read a Certificate of Analysis and verify it directly with the lab.
Prior authorizations, appeals, savings programs and cost comparisons.
Account questions, forum rules, posting etiquette and quick answers.
GLP-1 (glucagon-like peptide-1) is a gut hormone released after eating. It stimulates insulin secretion, suppresses glucagon, slows gastric emptying, and acts on appetite centers in the brain. GLP-1 receptor agonists are engineered analogues that resist breakdown, so a single weekly injection produces steady receptor activation.
Newer molecules add receptors: tirzepatide is a dual GIP/GLP-1 agonist, and retatrutide adds glucagon receptor activity on top — each addition has, so far, meant greater average weight reduction in trials.
Want the full picture with curves and sources? Open the Trial Data Explorer.
First GLP-1 agonist approved — twice-daily injection derived from Gila monster venom.
First GLP-1 approved specifically for chronic weight management.
Once-weekly dosing arrives; the modern era begins.
Semaglutide 2.4 mg approved for obesity after STEP-1 showed ~15% mean weight loss.
First dual GIP/GLP-1 agonist; SURMOUNT-1 reports ~21% mean weight loss.
Tirzepatide approved for obesity; SELECT shows a 20% cut in major cardiac events with semaglutide.
Orforglipron phase 3 readouts and retatrutide's TRIUMPH program point at the next generation.