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CompletedNCT03885297Updated Jun 18, 2024

3mg Liraglutide for Overweight or Obesity

An observational study in Overweight, Obesity and Infertility, Female, sponsored by University Hospitals Coventry and Warwickshire NHS Trust. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-18.

Sponsored by University Hospitals Coventry and Warwickshire NHS Trust · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
43
Ages
18 Years and older
Sex
All
01

Study summary

In this study investigators will investigate the beneficial metabolic sequelae of Liraglutide in patients with obesity or overweight; including changes in vital signs, anthropometric characteristics (weight, body mass index and body composition), biochemical parameters, metabolomics and micro-ribonucleotide acid (miRNA) molecules from blood tests. Liraglutide is a commercially available analogue of a gut hormone physiologically produced in our bowel in response to food, licenced for the treatment of overweight or obesity. Liraglutide will be offered to patients attending National Health System (NHS) or private clinics within indication and according to their agreed clinical management. Investigators aim to collect real-life information for this study along with planned clinical management from patients who agree to their treatment and to take part in our study. Patients will be able to withdraw from treatment and study at any time without giving any explanation.

If successful, this study will help us combine clinical, biochemical and molecular information which will allow us to gain deeper understanding on the mechanisms behind the beneficial metabolic effects of Liraglutide in overweight and obesity. Data generated from this study will hopefully help us acquire funding for a larger multicentre study; the results of which can have substantial impact on millions of people with overweight or obesity around the world.

Read the detailed description

1) Obesity is a global pandemic with debilitating consequences. It affects both adults and children; however, the prevalence of overweight and obesity among children and adolescents aged 5-19 has risen dramatically from just 4% in 1975 to just over 18% in 2016, highlighting the seriousness of this problem. The rise has occurred similarly among both boys and girls: in 2016 18% of girls and 19% of boys were overweight. While just under 1% of children and adolescents aged 5-19 were obese in 1975, more 124 million children and adolescents (6% of girls and 8% of boys) were obese in 2016.

Obesity is a major risk factor for noncommunicable diseases such as:

  1. Cardiovascular diseases (mainly heart disease and stroke), which were the leading cause of death in United States of America(USA);
  2. Diabetes Mellitus
  3. Musculoskeletal disorders (especially osteoarthritis - a highly disabling degenerative disease of the joints);
  4. Some forms of malignancy (including endometrial, breast, ovarian, prostate, liver, gallbladder, kidney, and colon);
  5. Infertility in both women and men. The risk for these noncommunicable diseases increases, with increases in Body Mass Index (BMI).

2) Liraglutide is a derivative of human incretin (metabolic hormone) glucagon-like peptide-1 (GLP-1) that is used as a long-acting glucagon-like peptide-1 receptor agonist, binding to the same receptors as does the endogenous metabolic hormone GLP-1 that stimulates insulin secretion. Liraglutide is licenced in USA and in European Union (EU), including United Kingdom (UK) for the management of Type 2 Diabetes Mellitus (T2DM) and Obesity or overweight when one or more metabolic co-morbidities are present.

Saxenda (3mg Liraglutide once daily) is an Food \& Drug Administration (FDA)-approved, prescription injectable Glucagon Like Peptide-1 (GLP-1) receptor agonist that, when used with a low-calorie diet and increased physical activity, can reduce excess weight in patients who are overweight (BMI ≥27Kg/m2) and additionally have weight-related medical problems (such as high blood pressure, high cholesterol, or insulin resistance/pre-diabetes), or obesity (BMI: >30Kg/m2) to lose weight. Saxenda is licensed and available in the UK for the management of obesity and overweight.

3) Metabolomics is the scientific study of chemical processes involving metabolites, the small molecule intermediates and products of metabolism. Specifically, metabolomics is the "systematic study of the unique chemical fingerprints that specific cellular processes leave behind", the study of their small-molecule metabolite profiles. The metabolome represents the complete set of metabolites in a biological cell, tissue, organ or organism, which are the end products of cellular processes. This in emerging area of metabolic research and in this study, will provide insight into the mechanisms through which 3mg Liraglutide improves weight and other metabolic sequelae (i.e glucose and lipids homeostasis) in humans during treatment. To the extend of our knowledge, there is a very limited number of such studies; none of which reporting on the effects of 3mg Liraglutide. Our collaborator Professor Gyanendra Tripathi has kindly agreed to fund costs for metabolomics analysis of our human samples. Metabolomics analysis of human serum or plasma samples is going to be performed by applying Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS). UPLC-MS assay will provide untargeted study of water-soluble metabolites (HILIC LCMS) and untargeted study of lipid metabolites (C18 reversed phase LCMS). Analysis is going to be performed at School of Biosciences, University of Birmingham.

4) MicroRNA (abbreviated miRNA) is a small non-coding RNA molecule (containing about 22 nucleotides) found in plants, animals and some viruses, that functions in RNA silencing and post-transcriptional regulation of gene expression. While most miRNAs are located within the cell, some miRNAs, commonly known as circulating miRNAs or extracellular miRNAs, have also been found in extracellular environment, including various biological fluids and cell culture media. MiRNAs play crucial roles in the regulation of stem cell progenitors differentiating into adipocytes. Studies to determine what role pluripotent stem cells play in adipogenesis, were examined in the immortalized human bone marrow-derived stromal cell line hMSC-Tert20. Decreased expression of miRNA-155, miRNA-221, and miRNA-222, have been found during the adipogenic programming of both immortalized and primary human Mesenchymal Stem Cells (hMSCs), suggesting that they act as negative regulators of differentiation. Conversely, ectopic expression of the miRNAs 155,221, and 222 significantly inhibited adipogenesis and repressed induction of the master regulators Peroxisome proliferator-activated receptor gamma(PPARγ) and CCAAT/enhancer-binding protein alpha (CEBPA). This paves the way for possible genetic obesity treatments. Our goal is however to see if treatment with 3mg Liraglutide will influence circulating miRNA levels. To the extent of our knowledge there is currently no study reporting this.

02

Conditions studied

  • Overweight
  • Obesity
  • Infertility, Female

Keywords

  • obesity
  • metabolism
  • liraglutide
  • saxenda
  • metabolomics
  • miRNA
  • weight loss
03

In context

Overweight

3,771 studies on the registry are indexed under Overweight; 863 are open to participants now.

This study's enrollment of 43 is below the median of 150 across 443 observational studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

University Hospitals Coventry and Warwickshire NHS Trust is the lead sponsor of 56 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Investigators don't anticipate any specific difficulties with recruitment for this study as overweight and obesity are very common conditions, and there are very few licensed medical options offering substantial weight loss. Liraglutide is one of them. Additionally, investigators don't see any specific difficulties in managing this study as it will be " part and parcel" of our patients' routine clinical visits. Liraglutide is going to be offered to our patients as per clinical need and the decision to treat them with liraglutide is going to be made before their potential participation in our study. Patients therefore are not going to be receiving treatment because of their participation in our study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult participants [age ≥18 y.o without upper age limit (to the discretion of the investigators)].
  • Body mass index (BMI) ≥ 30 kg/m2 without coexisting comorbidities or BMI ≥27Kg/m2 with comorbidities like hypertension, hyperlipidaemia, prediabetes or obstructive sleep apnoea.
  • Willing to comply with study requirements and able to give informed consent.

Exclusion criteria

Exclusion Criteria:

  • Type 1 or Type 2 diabetes mellitus
  • History of chronic or acute pancreatitis
  • Known active hepatitis or active liver disease
  • Symptomatic gallstones or kidney stones, acute cholecystitis or history of duodenal inflammatory diseases including Crohn's Disease and Celiac Disease
  • Persistent anaemia, defined as haemoglobin\<10 g/dl
  • Chronic or acute renal impairment (eGFR \<30 ml/min/1.73m2)
  • Active systemic infection (sepsis)
  • Active malignancy within the last 5 years, including any form of thyroid cancer (including sporadic or familial medullary thyroid cancer) or personal, or family history of Multiple Endocrine Neoplasia type 2.
  • Active illicit substance abuse or alcoholism
  • Current pregnancy or breastfeeding at screening or 6 months previously
  • Donated blood during the preceding 3 months or intention to do so before the end of the study.
  • Any other mental or physical condition which, in the opinion of the Investigator, makes the subject a poor candidate for clinical trial participation.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
43 participants (actual)
Patient registry
No

Groups and cohorts

  • Overweight/obese participants

    Patients will be recruited prospectively from the weight management and Polycystic Ovary Syndrome (PCOS) clinics at University Hospitals Coventry and Warwickshire (UHCW) NHS Trust following discussion with their treating physician, who will also be a member of the research team and joint agreement on initiation of treatment with 3mg Liraglutide once daily as per clinical management plan. Patients will additionally receive standard NHS Tier 3 lifestyle advice and support for the duration of the study. Lifestyle modification aimed at weight loss will be delivered by a dietician or other trained health care professional within individual sessions for a period of 6 months. Finally, all patients will be able to withdraw from treatment and/or the study at any point without giving any explanation. This will have no impact in their clinical management.

    Drug: Saxenda · Other: Lifestyle modification · Diagnostic Test: Metabolomics · Diagnostic Test: miRNA

Interventions

  • Obesity pharmacotherapy

  • OtherLifestyle modification

    Tier 3 NHS weight management

  • Diagnostic testMetabolomics

    Small molecule intermediates and products of metabolism

  • Diagnostic testmiRNA

    Small non-coding RNA molecules

06

What researchers measure

Primary outcomes

  1. Weight changes related to treatment

    Weight reduction in kilograms from baseline while on treatment with 3mg Liraglutide once daily in patients with overweight (BMI: ≥27Kg/m2) or obesity (BMI: ≥30Kg/m2) with regards to:

    Time frame: 6 months

Secondary outcomes

  1. Changes in fat and lean mass while on treatment

    Fat and lean mass changes in percentages from baseline using air displacement plethysmography and bioelectrical impedance techniques while on treatment with 3mg Liraglutide once daily for overweight and obesity

    Time frame: 6 months

  2. Changes in an untargeted study of water-soluble metabolites (HILIC LCMS) while on treatment

    Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) will be performed to measure plasma changes of water-soluble metabolites (HILIC LCMS).

    Time frame: 6 months

  3. Changes in an untargeted study of lipid metabolites (C18 reversed phase LCMS) while on treatment

    Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) will be performed to measure plasma changes of lipid metabolites (C18 reversed phase LCMS)

    Time frame: 6 months

  4. Changes in the expression of miRNA-155 while on treatment.

    Decreased expression of miRNA-155 has been found during the adipogenic programming of both immortalized and primary hMSCs, suggesting that it acts as negative regulators of fat cell differentiation. We will measure this in plasma.

    Time frame: 6 months

  5. Changes in the expression of miRNA-221 while on treatment.

    Decreased expression of miRNA-221 has been found during the adipogenic programming of both immortalized and primary hMSCs, suggesting that it acts as negative regulators of fat cell differentiation. We will measure this in plasma.

    Time frame: 6 months

  6. Changes in the expression of miRNA-222 while on treatment.

    Decreased expression of miRNA-222, has been found during the adipogenic programming of both immortalized and primary hMSCs, suggesting that it acts as negative regulators of fat cell differentiation. We will measure this in plasma.

    Time frame: 6 months

  7. Changes in glucose and insulin from baseline.

    We will measure changes in serum glucose and insulin from baseline while on treatment using ELISA (enzyme-linked immunosorbent assay).

    Time frame: 6 months

  8. Changes in systolic blood pressure.

    We will measure systolic blood pressure changes from baseline while on treatment.

    Time frame: 6 months

  9. Changes diastolic blood pressure.

    We will measure diastolic blood pressure changes from baseline while on treatment.

    Time frame: 6 months

  10. Changes in heart rate.

    We will measure heart rate changes from baseline.

    Time frame: 6 months

07

Study locations

1 site
  • WISDEM Centre, University Hospitals Coventry and Warwickshire
    Coventry, West Midlands CV2 2DX, United Kingdom
08

References and documents

Publications

  • James WP. WHO recognition of the global obesity epidemic. Int J Obes (Lond). 2008 Dec;32 Suppl 7:S120-6. doi: 10.1038/ijo.2008.247. PubMed 19136980 ↗
  • WHO annual report 2017; Obesity update - © OECD 2017
  • http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2010/ucm198638.htm
  • FDA approves weight-management drug Saxenda
  • Daviss, Bennett (April 2005).
  • Jordan KW, Nordenstam J, Lauwers GY, Rothenberger DA, Alavi K, Garwood M, Cheng LL. Metabolomic characterization of human rectal adenocarcinoma with intact tissue magnetic resonance spectroscopy. Dis Colon Rectum. 2009 Mar;52(3):520-5. doi: 10.1007/DCR.0b013e31819c9a2c. PubMed 19333056 ↗
  • Ambros V. The functions of animal microRNAs. Nature. 2004 Sep 16;431(7006):350-5. doi: 10.1038/nature02871. PubMed 15372042 ↗
  • Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004 Jan 23;116(2):281-97. doi: 10.1016/s0092-8674(04)00045-5. PubMed 14744438 ↗
  • Extracellular/Circulating MicroRNAs: Release Mechanisms, Functions and Challenges

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2019 to primary completion in Dec 2020, 23 months.

Of 145 non-industry observational studies under Overweight, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 132. This study's 23 months is below that.

Counting every sponsor, half of 164 studies reached it within 38 months; a quarter within 15 and three quarters within 98.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 27, 2019
First posted
Mar 21, 2019
StartActual
Jan 18, 2019
Primary completionActual
Dec 18, 2020
CompletionActual
Dec 18, 2020
Last update
Jun 18, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03885297
Lead sponsor
University Hospitals Coventry and Warwickshire NHS Trust
Collaborators
Kingston University, University of Warwick, University of Birmingham
Responsible party
Sponsor
First posted
Mar 21, 2019
Start date
Jan 18, 2019
Primary completion
Dec 18, 2020
Completion
Dec 18, 2020
Last update
Jun 18, 2024

Study contacts

Georgios K. Dimitriadis
principal investigator · University Hospitals Coventry and Warwickshire NHS Trust

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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