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Quality assessment of included studies A study by Richard et al

But that is inaccurate

Assuming the remaining Phase 3 data continues to support both safety and efficacy, and the FDA review process moves forward without delays, industry projections currently point to a possible late 2026 to 2027 timeline

Main measures The incidence of intestinal obstruction was compared between GLP-1RAs and each of six other classes of non-GLP-1RA anti-diabetic medications

Furthermore, changes in body composition, particularly with regard to muscle mass, may have influenced the energy expenditure findings, highlighting the need for longer-term studies to fully assess the effects of GLP-1 analogs on metabolism