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ACTIVE NOT RECRUITINGPhase3

Efficacy and Safety of MET097 Once-Weekly in People With Overweight or Obesity

Sponsor: Pfizer

NCT ID: NCT07311850

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
MET097 (drug), Placebo (drug)
How long the study runs
Study runs about 28 months (dates as stated)
About the drug or intervention
MET097 — drug: Once-weekly MET097 administered via subcutaneous injection · Placebo — drug: Once-weekly placebo administered via subcutaneous injection
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
3,578
Started
2025-12-19
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for obesity and overweight
  • • Phase3 - 3,578 participants
  • • This study investigates the efficacy and safety of once weekly injectable MET097 in adult participants with obesity or overweight with weight-related comorbidities excluding T2D

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with obesity and overweight

Where?

  • • Sandbach - Ashfields Primary Care Center
  • • Hendon - Civia Health Sunderland
  • • Glasgow - FutureMeds Glasgow McCafferty House
  • • Bellshill - Synexus Glasgow Clinical Research Centre
  • • +20 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

This study investigates the efficacy and safety of once weekly injectable MET097 in adult participants with obesity or overweight with weight-related comorbidities excluding T2D. This trial will last for a duration of 84 weeks. The primary endpoint will be assessed after 64 weeks of treatment with the secondary at 84 weeks.

Obesity and Overweight

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Who cannot take part

  • ✗Have any form of diabetes
  • ✗Have a self-reported body weight change \> 5 kg (11 pounds) within 3 months prior to Screening
  • ✗Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2)
  • ✗History of chronic pancreatitis or presence of acute pancreatitis within the past 180 days prior to the Screening...
See the full criteria
Inclusion Criteria: * BMI ≥ 30 kg/m2 or BMI ≥ 27.0 kg/m2 to \<30.0 kg/m2 and presence of at least 1 of the following weight- related comorbidities: Hypertension, dyslipidemia, obstructive sleep apnea, or cardiovascular disease) Exclusion Criteria: * Have any form of diabetes * Have a self-reported body weight change \> 5 kg (11 pounds) within 3 months prior to Screening * Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2) * History of chronic pancreatitis or presence of acute pancreatitis within the past 180 days prior to the Screening visit; or active/current, symptomatic gallbladder disease

Where Is This Study? (24 UK sites)

Ashfields Primary Care Center

Sandbach CW11 1EQ, United Kingdom

Civia Health Sunderland

Hendon SR1 1PB, United Kingdom

FutureMeds Glasgow McCafferty House

Glasgow G20 7BE, United Kingdom

Synexus Glasgow Clinical Research Centre

Bellshill ML4 3NJ, United Kingdom

FutureMeds Birmingham

Birmingham B21 9RY, United Kingdom

Hospital R&D contact (matched)

Sarah Pountain Head of Research Governance

R&D@uhb.nhs.uk0121 371 4185

Civia Health_Boots Birmingham

Birmingham B4 7TA, United Kingdom

Hospital R&D contact (matched)

Sarah Pountain Head of Research Governance

R&D@uhb.nhs.uk0121 371 4185

Southmead Hospital

Bristol BS10 5NB, United Kingdom

Hospital R&D contact (matched)

Helen Lewis-White

Research@nbt.nhs.uk0117 41 49330

FutureMeds Liverpool

Bromborough CH62 6EE, United Kingdom

Synexus Midlands Clinical Research Centre

Edgbaston B16 8QQ, United Kingdom

Panthera Biopartners Limited - Enfield

Enfield EN3 4GS, United Kingdom

Panthera Biopartners Limited - Glasgow

Glasgow G51 4TY, United Kingdom

Bodyline Medical Clinic, Crosby Civia Health

Liverpool L22 4QQ, United Kingdom

FutureMeds London

London NW10 2PB, United Kingdom

Synexus Manchester Clinical Research Centre

Manchester M15 6SE, United Kingdom

Hospital R&D contact (matched)

Elizabeth Mainwaring

R&D.applications@mft.nhs.uk0161 276 3340

Kiltearn Medical Centre

Nantwich CW5 5NX, United Kingdom

FutureMeds Newcastle upon Tyne

Newcastle upon Tyne NE6 1SG, United Kingdom

Hospital R&D contact (matched)

Research and Development

nuth.genericqueries@nhs.net0191 282 4926

Civia Health_Boots Nottingham

Nottingham NG1 3QS,, United Kingdom

Hospital R&D contact (matched)

Alison Lloyd

nuhnt.researchsponsor@nhs.net0115 9249924

Panthera Biopartners Limited - Preston

Preston PR2 9QB, United Kingdom

Panthera Biopartners Limited - Rochdale

Rochdale OL11 4AU, United Kingdom

Clifton Medical Centre

Rotherham S65 2EN, United Kingdom

Panthera Biopartners Limited - Sheffield

Sheffield S2 5FX, United Kingdom

Hospital R&D contact (matched)

Alessia Dunn

STH.ResearchAdministration@nhs.net0114 2712550

Bodyline Medical Clinic, St Helens Civia Health

St Helens WA9 1AF, United Kingdom

FutureMeds Teesside

Stockton TS19 8PE, United Kingdom

Panthera Biopartners Limited - York

York YO24 4LJ, United Kingdom

Data sourced from ClinicalTrials.gov · Last verified: 2026-09