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Exploring the Use of GLP-1-Based Interventions for Obesity: A Qualitative Analysis of ClinicalTrials.gov Data
Nouf M Alourfi1, Nasser M Alorfi2
1Department of Chemistry, Arts and Sciences College, Rabigh Campus, King Abdulaziz University, Jeddah, Rabigh, 21589, Saudi Arabia.
Background:
Glucagon-like peptide-1 (GLP-1) receptor agonists are a key pharmacological target in obesity management, associated with sustained weight loss and broader metabolic benefits beyond glycaemic control.
Objective:
To analyse the characteristics, design trends, and research themes of completed clinical trials investigating GLP-1-based interventions for obesity registered in ClinicalTrials.gov.
Methods:
A registry-based cross-sectional qualitative analysis was conducted using ClinicalTrials.gov data retrieved on October 18, 2025. Completed interventional trials evaluating GLP-1 receptor agonists, including liraglutide, semaglutide, tirzepatide, exenatide, dulaglutide, and lixisenatide, were identified. Extracted variables included study phase, intervention type, enrolment, primary outcomes, and completion year. Descriptive statistics were used to summarize quantitative data, and qualitative thematic synthesis was applied to categorize outcome domains and research focus.
Results:
A total of 227 completed interventional studies were identified. Liraglutide was the most frequently investigated agent (n = 86), followed by semaglutide (n = 18), tirzepatide (n = 18), exenatide (n = 15), and other GLP-1 analogues. Phase 3 and 4 trials predominated, with most studies enrolling fewer than 200 participants. Primary outcomes were mainly weight-related, with increasing attention to hepatic, cardiometabolic, and inflammatory endpoints. A marked rise in completed trials was observed after 2018, corresponding with the introduction of newer GLP-1 analogues.
Conclusion:
Completed GLP-1 obesity trials demonstrate an expanding research focus from weight and glycaemic control toward broader metabolic and organ-specific outcomes. This registry-based qualitative analysis provides a novel overview of research maturity and evolving priorities in GLP-1-based obesity pharmacotherapy.
Insights
Glucagon-like peptide-1 (GLP-1) receptor agonists are crucial for obesity treatment, showing sustained weight loss and metabolic benefits. Research trends reveal a shift towards broader metabolic and organ-specific outcomes beyond initial glycaemic control.
Area of Science:
- Pharmacology
- Endocrinology
- Clinical Research
Background:
- Glucagon-like peptide-1 (GLP-1) receptor agonists are a cornerstone in obesity pharmacotherapy.
- These agents offer significant weight loss and metabolic advantages beyond glycemic control.
Purpose of the Study:
- To analyze characteristics, design trends, and research themes of completed clinical trials for GLP-1-based obesity interventions.
- To provide an overview of research maturity and evolving priorities in GLP-1 obesity pharmacotherapy.
Main Methods:
- Registry-based cross-sectional qualitative analysis of ClinicalTrials.gov data.
- Included completed interventional trials of GLP-1 receptor agonists for obesity.
- Extracted data on study phase, intervention, enrollment, outcomes, and completion year; thematic synthesis used.
Main Results:
- 227 completed trials identified; liraglutide most studied, followed by semaglutide and tirzepatide.
- Phase 3 and 4 trials predominated, typically with <200 participants.
- Primary outcomes evolved from weight-centric to include hepatic, cardiometabolic, and inflammatory markers, with a surge post-2018.
Conclusions:
- Completed GLP-1 obesity trials show an expanding research scope.
- Focus is shifting from weight and glycemic control to comprehensive metabolic and organ-specific outcomes.
- This analysis highlights evolving research priorities in GLP-1 obesity pharmacotherapy.
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