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Weekly GLP-1 Receptor Agonists in Obese Individuals Without Diabetes
Plain-language guide to NCT07834398: phase 3 randomized trial of Tirzepatide and Dulaglutide, 150 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT07834398
- Phase
- phase 3
- Status
- completed
- Start
- 2025-11-14
- Completion (planned or actual)
- 2026-04-13
- Participants
- 150 (actual)
- Design
- randomized, open label (everyone knows who gets what), treatment
- Conditions studied
- Non-diabetec Obesity; Obesity (Disorder)
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
The trial (phase 3) is built around Tirzepatide and Dulaglutide.
It had three arms (groups): Dulaglutide Group (active comparator), Semaglutide Group (active comparator) and Tirzepatide Group (active comparator).
The registry classes the interventions as drug.
More on the Plan
Monthly follow-up will ensure medication adherence and monitor gastrointestinal adverse events.
Inclusion: BMI \>30, age \>18, non-diabetic.
Exclusion: Diabetes, liver disease, renal dysfunction, pancreatic disease, thyroid disease, psychological disorders, pregnancy.
Who Took Part
150 actual participants took part.
It was open to people of any sex aged from 18 years up to 65 years.
Healthy volunteers could join, not only people with the condition.
Examples of who could join: Subjects (above 18 years old) obese body mass index (BMI) above 30.
The full record lists 1 inclusion and 1 exclusion criteria; among the exclusions: subjects with liver disease, renal dysfunction diabetes, pancreatic diseases ,thyroid disorder or goiter psychological diseases like depression and pregnant women, and patients who will refuse.
How the Study Was Run
The set-up was randomized, parallel-group and open-label.
Random assignment meant chance, not the researchers, decided who got Tirzepatide and who got the comparison, which limits bias.
Groups ran in parallel: each of the participants stayed in one arm throughout.
Everyone knew when Tirzepatide was being given (open label), which is simpler to run but leaves more room for expectations to affect what is reported.
It started in 2025-11-14 with completion listed for 2026-04-13.
It ran at 1 site in Saudi Arabia.
Its stated primary purpose is treatment.
What Was Measured
The main thing measured (primary outcome): change in body weight at 3 and 6 months (time frame: Baseline, Week 12 (3 months) and Week 24 (6 months)).
It also tracked 8 secondary outcomes, for example Change in Body Mass Index (BMI), Change in Glycated Hemoglobin (HbA1c), Change in Low-Density Lipoprotein Cholesterol (LDL-C), Change in Triglycerides, Change in High-Density Lipoprotein Cholesterol (HDL-C) and Change in Total Cholesterol (TC).
What This Means in Plain Language
Put simply, this is a phase 3, randomized trial of Tirzepatide and Dulaglutide in 150 people.
The trial is marked completed; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Tirzepatide compound page and the Dulaglutide compound page, all human trials.
Our Notes on the Compounds
Tirzepatide: A prescription peptide medicine that acts on both the GIP and GLP-1 receptors; Mounjaro and Zepbound contain the same active ingredient.
Dulaglutide: A once-weekly GLP-1 receptor agonist (two GLP-1 analog chains joined to an antibody Fc fragment), sold as Trulicity.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.