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Clinical Trials in Taiwan / NCT06660173
Active, not recruiting Phase 2

A Study of Maridebart Cafraglutide in Adult Participants With Type 2 Diabetes Mellitus (T2DM)

NCT06660173 · tracked via the Priya Life Science Taiwan tracker
Sponsor
Phase
Phase 2
Started
2024-11-07
Last updated
2026-09-11

Condition(s) studied

Type 2 Diabetes Mellitus (T2DM)

Investigational drug(s) / intervention(s)

Maridebart Cafraglutide →Placebo

Maridebart Cafraglutide: Solution for subcutaneous injection.

Placebo: Solution for subcutaneous injection.

Study summary

The main purpose of this study is to assess the dose-response relationship of maridebart cafraglutide on glucose control compared with placebo.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years at screening (or ≥ legal age within the country if it is older than 18 years) * Type 2 diabetes for ≥6 months according to the World Health Organization classification * HbA1c of 7.0% to 10.5%, inclusive, as assessed by the central laboratory * Treatment of diabetes with diet and exercise alone, or with a stable dose of metformin, with or without a sodium-glucose cotransporter-2 inhibitor, for at least 3 months prior to screening * Body mass index of 23 to 50 kilograms per square meter Exclusion Criteria: * Type 1 diabetes * Use of any glucose-lowering medication, other than metformin with or without a sodium-glucose cotransporter-2 inhibitor, within 3 months prior to screening * Estimated glomerular filtration rate (eGFR) \<30 milliliters/minute/1.73 square meter, calculated by the Chronic Kidney Disease-Epidemiology equation. * Uncontrolled and potentially unstable diabetic retinopathy or maculopathy * History of acute or chronic pancreatitis * Malignancy within 5 years before screening, except for nonmelanoma skin cancer, in situ carcinoma of the cervix, or in situ prostate cancer * Myocardial infarction, unstable angina, coronary artery bypass graft surgery or other major cardiovascular surgery, percutaneous coronary intervention, transient ischemic attack, cerebrovascular accident, or decompensated congestive heart failure within 90 days prior to screening, or currently have New York Heart Association Class III or IV heart failure. * Use of medications that affect glucose control or body weight or history of bariatric surgery or procedures.

Primary outcome measure(s)

Trial sites (96)

FacilityCityRegionStatus
Accel Research Site - Birmingham Clinical Research Unit Birmingham Alabama
Anaheim Clinical Trials Anaheim California
Hope Clinical Research LLC Canoga Park California
Orange County Research Center Lake Forest California
San Jose Clinical Trials San Jose California
Northeast Research Institute - Neri Fleming Island Florida
New Horizon Research Center Miami Florida
Florida Institute for Clinical Research Orlando Florida
Conquest Research - Winter Park Winter Park Florida
Accel Research Site - Neurostudies Decatur Georgia
Cedar Crosse Research and Health Care Chicago Illinois
Tandem Clinical Research - Marrero Marrero Louisiana
DM Clinical - Detroit Southfield Michigan
Montana Medical Research Missoula Montana
Physicians East Greenville North Carolina
Diabetes and Endocrinology Associates of Stark County Inc Canton Ohio
Alliance for Multispecialty Research Norman Oklahoma
Trial Management Associates - Myrtle Beach Myrtle Beach South Carolina
FutureSearch Trials of Neurology Austin Texas
Velocity Clinical Research - Dallas Dallas Texas
DM Clinical Research - Cyfair Clinical Research Center Houston Texas
Southern Endocrinology Associates PA Mesquite Texas
Be Well Clinical Studies Round Rock Texas
Diabetes and Glandular Disease Clinic San Antonio Texas
DM Clinical Research - Martin Diagnostic Clinic Tomball Texas
Charlottesville Medical Research Center Charlottesville Virginia
Manassas Clinical Research Center Inc Manassas Virginia
Eastside Research Associates Health Research Redmond Washington
Medizinische Universitaet Graz Graz Austria
Krankenhaus der Barmherzigen Brueder Linz Linz Austria
Universitaetsklinikum Allgemeines Krankenhaus Wien Vienna Austria
Klinik Hietzing Vienna Austria
Laiko General Hospital of Athens Athens Greece
Athens Medical Center S.A - Iatriko Amarousiou Marousi Greece
Athens Medical Center- Iatriko Paleou Falirou Palaió Fáliro Greece
Geniko Nosokomeio Peiraia Tzaneio Piraeus Greece
General Hospital of Thessaloniki Ahepa Thessaloniki Greece
Thermi Clinic S.A. Thessaloniki Greece
Queen Mary Hospital, The University of Hong Kong Hong Kong Hong Kong
Lausmed Kft Baja Hungary

+ 56 more sites — see the full list on the official registry below.

More Amgen trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06660173 on ClinicalTrials.gov ↗ ← All trials in Taiwan