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NCT06926842CompletedPhase 2

Efficacy and Safety of Petrelintide in Participants With Overweight or Obesity and Type 2 Diabetes (ZUPREME 2)

A Randomized, Double-Blind, Phase 2 Trial of Once-Weekly Petrelintide Compared With Placebo in Participants With Overweight or Obesity and Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 9 Sept 2026

Brief summary (registry, in English)

The main purpose of this study is to investigate efficacy and safety of three doses of petrelintide versus placebo in participants with overweight or obesity and type 2 diabetes.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
221 (actual)
First submitted
11 Apr 2025
Start date
22 Apr 2025
Primary completion date
13 Aug 2026
Lead sponsor
Zealand Pharma
NCT number
NCT06926842

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 221
  • From 22 Apr 2025 to the primary completion date, 13 Aug 2026
  • 48 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Main Inclusion Criteria:
  • Male or female participants with body mass index (BMI) ≥27.0 kg/m2.
  • Diagnosed with type 2 diabetes ≥180 days prior to the day of screening.
  • Treated with metformin with or without sodium-glucose cotransporter 2 inhibitors. Treatment should be stable (same drug\[s\], dose, and dosing frequency) for at least 90 days prior to screening.
    • Main Exclusion Criteria:
  • Severe hypoglycemia within 6 months prior to screening or history of hypoglycemia unawareness.
  • Receipt of any other glucose-lowering drug than those listed in the inclusion criterion within 90 days prior to screening.
  • A self-reported change in body weight \>5% within 90 days prior to screening, irrespective of medical records.
  • Treatment with any medication (prescribed or over-the-counter) or alternative remedies (herbal or nutritional supplements) intended to promote weight loss within 90 days prior to screening.
  • Previous or planned (during the trial period) obesity treatment with surgery or a body weight loss device. However, liposuction or surgical removal of fat depots more than 1 year prior to screening or device-based interventions (e.g., sleeve, banding, or similar) that have been removed more than 6 months prior to screening, are allowed.
  • Obesity due to endocrine disorders or genetic syndromes.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (48)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
M3 Wake Research - Atlanta
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Elligo Clinical Research, Inc.
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AustinUnited StatesUnknown status
Mercury Street Medical Group, PLLC
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ButteUnited StatesUnknown status
East Coast Institute for Research - Canton
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CantonUnited StatesUnknown status
AZ Endocrine Institute
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ChandlerUnited StatesUnknown status
M3 Wake Research - Charleston
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CharlestonUnited StatesUnknown status
Javara Inc
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CharlotteUnited StatesUnknown status
M3 Wake Research/ClinSearch, LLC
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ChattanoogaUnited StatesUnknown status
Great Lakes Clinical Trials
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ChicagoUnited StatesUnknown status
Velocity Clinical Research, Cincinnati, Mt. Auburn
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CincinnatiUnited StatesUnknown status
Innovative Research of West Florida
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ClearwaterUnited StatesUnknown status
Centricity Research
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ColumbusUnited StatesUnknown status
Cullman Clinical Trials - Family Medicine
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CullmanUnited StatesUnknown status
The University of Texas Southwestern Medical Center
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DallasUnited StatesUnknown status
AAMRC
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FlintUnited StatesUnknown status
PharmQuest Life Sciences LLC
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GreensboroUnited StatesUnknown status
Velocity Clinical Research, Gulfport
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GulfportUnited StatesUnknown status
Juno Research, LLC
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HoustonUnited StatesUnknown status
Velocity Clinical Research
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Huntington ParkUnited StatesUnknown status
Tekton Research, LLC
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IrvingUnited StatesUnknown status
Solutions Through Advanced Research, Inc
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JacksonvilleUnited StatesUnknown status
East Coast Institute for Research, LLC
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JacksonvilleUnited StatesUnknown status
AMR Kansas City
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Kansas CityUnited StatesUnknown status
M3 Wake Research - Lake City
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Lake CityUnited StatesUnknown status
Palm Research Center Inc
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Las VegasUnited StatesUnknown status
M3 Wake Research - Las Vegas, NV
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Las VegasUnited StatesUnknown status
Medical Investigation Inc
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Little RockUnited StatesUnknown status
Manaasas Clinical Research Center
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ManassasUnited StatesUnknown status
Tekton Research, LLC
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McKinneyUnited StatesUnknown status
International Diabetes Center
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MinneapolisUnited StatesUnknown status
DelRicht Research - New Orleans
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New OrleansUnited StatesUnknown status
Lynn Institute of Norman
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NormanUnited StatesUnknown status
Velocity Clinical Research - North Hollywood
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North HollywoodUnited StatesUnknown status
West Orange Endocrinology P.A.
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OcoeeUnited StatesUnknown status
Elite Clinical Studies, LLC
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PhoenixUnited StatesUnknown status
M3 Wake Research
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RaleighUnited StatesUnknown status
Exalt Clinical Research
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San DiegoUnited StatesUnknown status
Texas Health Care, PLLC
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San MarcosUnited StatesUnknown status
Privia Medical Group Georgia, LLC
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SavannahUnited StatesUnknown status
Consano Clinical Research
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Shavano ParkUnited StatesUnknown status
Texas Health Care
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StephenvilleUnited StatesUnknown status
M3 Wake Research, Tucson Neuroscience Research, LLC
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TucsonUnited StatesUnknown status
Diablo Clinical Research, Inc.
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Walnut CreekUnited StatesUnknown status
Emerson Clinical Research
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Washington D.C.United StatesUnknown status
Chase Medical Research, LLC
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WaterburyUnited StatesUnknown status
Iowa Diabetes & Endocrinology Research Center
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West Des MoinesUnited StatesUnknown status
Palm Beach Research Center
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West Palm BeachUnited StatesUnknown status
Heartland Research Associates, LLC
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WichitaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.