Ribupatide
Ribupatide (also known as HRS9531 or KAI-9531) is an investigational dual GLP-1 and GIP receptor agonist currently in Phase 3 clinical trials. Research demonstrates its potential to induce significant weight loss and improve metabolic markers in individuals with obesity and type 2 diabetes, with both once-weekly injectable and once-daily oral formulations under investigation.
01Dosing reference
02Mechanism of action
Dual Receptor Activation
Ribupatide binds to and activates both the glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) receptors.
Metabolic Regulation
Activation of these receptors enhances glucose-dependent insulin secretion, slows gastric emptying, and signals satiety in the brain.
Weight Loss and Glycemic Control
This dual action leads to reduced food intake, improved blood sugar levels, and significant reductions in body weight.
03Human evidence
Significant weight loss in Phase 2 trials
A Phase 2 clinical trial of once-daily oral ribupatide demonstrated weight loss of up to 12.1% in adults with obesity.
Efficacy in Phase 3 trials
Once-weekly subcutaneous injections of ribupatide are being evaluated in global Phase 3 trials (such as the KAINETIC program) for obesity and weight management.
04Preclinical evidence
Receptor binding affinity
In vitro studies demonstrated that ribupatide effectively binds to both GLP-1 and GIP receptors, showing potent dual agonism.
Metabolic improvements in animal models
Preclinical animal models of obesity and diabetes showed reduced food intake and improved glycemic control following ribupatide administration.
05What is known vs. unknown
- Ribupatide is a synthetic peptide acting as a dual GLP-1/GIP receptor agonist.
- It is being developed in both once-weekly subcutaneous injection and once-daily oral formulations.
- Clinical trials have shown it can achieve significant weight loss, with some studies reporting over 12% reduction in body weight.
- It is currently advancing through Phase 3 clinical trials for the treatment of obesity and type 2 diabetes.
- Long-term safety and cardiovascular outcomes of ribupatide are still being evaluated in ongoing Phase 3 trials.
- The exact differences in efficacy and tolerability between its oral and injectable formulations require further large-scale comparison.
- It is not yet FDA-approved and remains an investigational drug.
06Safety & regulatory context
07Compared with Tirzepatide
08Glossary
09Knowledge check
10Sources
- ClinicalTrials.gov Efficacy and Safety of Ribupatide (KAI-9531) in Obesity
- Journal Efficacy and Safety of Oral Ribupatide (HRS9531)
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