Retatrutide for Type 2 Diabetes: Does It Work?
Evidence-based review of Retatrutide's effectiveness for type 2 diabetes, including mechanism of action, dosage context, clinical data, and realistic expectations.
How Retatrutide Addresses Type 2 Diabetes
Retatrutide's GLP-1 and GIP agonism improves glycemic control by enhancing glucose-dependent insulin secretion, reducing glucagon secretion when glucose is elevated, and slowing gastric emptying to blunt post-meal glucose spikes. Phase 2 data showed significant HbA1c reductions alongside weight loss.
What Retatrutide Is Primarily Used For
- 1.Weight loss
- 2.Obesity management
- 3.Metabolic syndrome
- 4.Type 2 diabetes (investigational)
What the Research Shows
Below is a summary of clinical evidence for Retatrutide. Note that not all trials specifically study type 2 diabetes as an endpoint.
24mg dose achieved mean body weight reduction of 24.2% at 48 weeks — the highest ever recorded for any injectable weight-loss drug in a clinical trial at the time.
Phase 3 trials ongoing. Expected to seek FDA approval in 2026–2027.
Realistic Expectations
Dosage Context for Type 2 Diabetes
Typical range: 1–24 mg, Once weekly
Administered as subcutaneous injection once weekly. Titrate slowly to minimize GI side effects. The TRIUMPH-1 trial used titration from 2mg up to 24mg over 24 weeks.
Doses for type 2 diabetes may vary from general guidelines. Consult a healthcare provider for condition-specific dosing.
Legal Status & Access
Investigational (not yet FDA approved). Not legally available for human use outside of clinical trials in the US.