Retatrutide Outperforms Ozempic in Diabetes Trial, But Side Effects Persist

2 min read
Source: USA Today
Retatrutide Outperforms Ozempic in Diabetes Trial, But Side Effects Persist
Photo: USA Today
TL;DR

Eli Lilly reported that its experimental drug retatrutide produced more than double the weight loss of Novo Nordisk's Ozempic in a Phase 3 trial for Type 2 diabetes. Over 80 weeks, participants lost 44 to 47 pounds on retatrutide versus 21 pounds on Ozempic. While retatrutide showed superior blood sugar control, it had higher discontinuation rates due to gastrointestinal side effects. Lilly plans to seek FDA approval in early 2027.

Key points

  • Retatrutide users lost an average of 44.3 to 47.4 pounds, compared to 20.9 pounds for Ozempic users.
  • A1C levels dropped by 2.2% for retatrutide versus 1.8% for Ozempic.
  • Discontinuation due to side effects was 7.9% for the 12mg retatrutide dose versus 2.7% for Ozempic.
  • Retatrutide is a triple agonist mimicking GIP, GLP-1, and glucagon, whereas Ozempic targets only GLP-1.

Background

This follows recent reports of retatrutide's benefits for sleep apnea and warnings about contaminated black-market versions. The current trial adds to a growing body of evidence regarding next-generation GLP-1 therapies.

How outlets are covering it

USA Today and ABC News emphasized the superior efficacy of retatrutide in weight loss and blood sugar control. WXLV highlighted the trade-off, noting that while retatrutide offered better results, it caused more side effects, leading to higher dropout rates. Novo Nordisk's spokesperson countered that Ozempic offers broader organ protection and a longer safety profile, noting its use by 28 million people worldwide.

Why it matters

The results suggest a potential shift in the market for obesity and diabetes treatments, with retatrutide offering more potent effects but requiring careful management of side effects. This could impact future prescribing guidelines and patient choices.

What to watch

Eli Lilly intends to submit retatrutide for FDA approval in early 2027. Detailed results will be presented at a future medical meeting and published in a peer-reviewed journal. Novo Nordisk is also awaiting approval for its experimental drug CagriSema by the end of 2026.

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