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Efficacy and Safety of Orforglipron in Obese Adults With or Without Diabetes: A Systematic Review and Meta-Analysis
Ravi Kumar Pandey1, Mahnoor Jan2, Aqsa Mohammad3
1Nepalgunj Medical College, Nepalgunj, Lumbini Province, Nepal.
Background:
Obesity represents a major global health challenge, contributing substantially to cardiovascular disease and metabolic complications. Orforglipron, a novel oral non-peptide GLP-1 receptor agonist, has emerged as a promising therapeutic option for weight management and glycemic control. This meta-analysis evaluated the efficacy and safety of orforglipron in obese patients with or without type 2 diabetes mellitus (T2DM).
Methods:
A comprehensive literature search was conducted across PubMed, Embase, Cochrane Library and ClinicalTrials.gov from inception to October 2025 to identify randomised controlled trials (RCTs) evaluating orforglipron in obese patients. Mean differences (MDs) and risk ratios (RRs) with 95% confidence intervals (CIs) were calculated using random-effects models.
Results:
Five RCTs comprising 4410 participants were included. Orforglipron demonstrated dose-dependent reductions in body weight from 2.48% at 3 mg to 9.8% at 45 mg, BMI from 0.89 to 3.62 kg/m2, waist circumference from 1.57 to 6.9 cm, and HbA1c from 0.76% to 1.04% compared with placebo. Favourable lipid changes included reductions in total cholesterol (MD: -4.51% [95% CI: -6.91 to -2.11]), LDL-C (MD: -5.34% [95% CI: -7.10 to -3.58]), and triglycerides (MD: -10.07% [95% CI: -12.33 to -7.80]), with increased HDL-C (MD: 2.94% [95% CI: 1.38 to 4.49]). However, gastrointestinal adverse events were significantly more frequent at doses of 12 mg or higher and treatment discontinuation rates were highest at 24 mg (RR:4.61 [95% CI:1.6 to 13.33]) and 36 mg (RR:3.68 [95% CI:2.48 to 5.44]) doses. Serious adverse events and mortality rates were comparable to those with placebo.
Conclusion:
Orforglipron significantly improved glycemic and lipid parameters in patients with obesity, demonstrating dose-dependent efficacy with maximal benefits at higher doses. While gastrointestinal tolerability remains a clinically important limitation requiring mitigation strategies, orforglipron represents a promising oral therapeutic option for comprehensive obesity and metabolic management.
Insights
Orforglipron, an oral GLP-1 agonist, effectively reduces weight, BMI, and HbA1c in obese patients. While higher doses show greater benefits, gastrointestinal side effects increase, necessitating careful management for this promising obesity treatment.
Area of Science:
- Metabolic disorders
- Pharmacology
- Cardiovascular health
Background:
- Obesity is a significant global health issue linked to cardiovascular and metabolic diseases.
- Orforglipron, an oral non-peptide GLP-1 receptor agonist, offers a potential new treatment for weight and glycemic control.
Purpose of the Study:
- To assess the efficacy and safety of orforglipron in obese individuals, with or without type 2 diabetes mellitus (T2DM).
Main Methods:
- A meta-analysis of five randomized controlled trials (RCTs) involving 4410 participants was conducted.
- Data were sourced from comprehensive literature searches of major databases up to October 2025.
- Random-effects models were used to calculate mean differences (MDs) and risk ratios (RRs) with 95% confidence intervals (CIs).
Main Results:
- Orforglipron showed dose-dependent reductions in body weight (up to 9.8%), BMI, and waist circumference.
- Significant improvements were observed in HbA1c (up to 1.04%), total cholesterol, LDL-C, and triglycerides, with increased HDL-C.
- Gastrointestinal adverse events were more frequent at doses ≥12 mg, and treatment discontinuation rates were highest at 24 mg and 36 mg.
Conclusions:
- Orforglipron effectively improves glycemic and lipid profiles in obese patients, with benefits increasing at higher doses.
- Gastrointestinal tolerability is a key limitation, but orforglipron shows promise as an oral therapy for obesity and metabolic management.
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