Evidence mapPaperPMID 41296780Full record

SynthesisEndocrinology, diabetes & metabolism2025

Efficacy and Safety of Orforglipron in Obese Adults With or Without Diabetes: A Systematic Review and Meta-Analysis.

Ravi Kumar Pandey, Mahnoor Jan, Aqsa Mohammad, Khawaja Arham Jawaid, Mawra Naveed, Muhammad Ali Abid, Abdullah Bin Amir, Shafique Ahmed, Muhammad Safiullah, Muhammad Imaz Bhatti and 5 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Endocrinology, diabetes & metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Ravi Kumar PandeyNepalgunj Medical College, Nepalgunj, Lumbini Province, Nepal.
Mahnoor JanShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Aqsa MohammadRawalpindi Medical University, Rawalpindi, Pakistan.
Khawaja Arham JawaidSharif Medical City Hospital, Lahore, Pakistan.
Mawra NaveedShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Muhammad Ali AbidKing Edward Medical University, Lahore, Pakistan.
Abdullah Bin AmirKing Edward Medical University, Lahore, Pakistan.
Shafique AhmedInternational University of Kyrgyzstan, Bishkek, Kyrgyzstan.
Muhammad SafiullahKing Edward Medical University, Lahore, Pakistan.ORCID 0009-0003-7773-2605
Muhammad Imaz BhattiKing Edward Medical University, Lahore, Pakistan.ORCID 0009-0000-9381-0106
Sana IftikharShaikh Khalifa Bin Zayed Al-Nahyan Medical and Dental College, Lahore, Pakistan.
Muhammad Nabeel SaddiqueKing Edward Medical University, Lahore, Pakistan.
Widyan AlfalhDar Alhekma Hospital, Benghazi, Libya.
Rihab Mohammed Bin OmarUniversity of Tripoli, Tripoli, Libya.
Husam Abu DawoodPalestine Polytechnic University, Hebron, Palestine.ORCID 0009-0005-3109-2600

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity 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).

methodsA 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.

resultsFive 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/m

conclusionOrforglipron 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.

Indexed as

Diabetes Mellitus, Type 2ObesityAdultFluorine CompoundsHumansOxadiazolesRandomized Controlled Trials as TopicTreatment OutcomeFluorine CompoundsorforglipronOxadiazolesGLP‐1 receptor agonistglycemic controlmeta‐analysisobesityorforgliprontype 2 diabetes mellitus

Identifiers

PMID41296780
PMCPMC12653021

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.