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Last updated 16 days ago
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A Master Protocol of Multiple Agents in Adults With Metabolic Dysfunction-Associated Steatotic Liver Disease (SYNERGY-Outcomes)
4500 patients around the world
Available in
Brazil, Argentina, United States, Mexico
Eli Lilly and Company
21
Research sites
4500
Patients around the world
This study is for people with
Fatty Liver
Hepatic Steatosis
Requirements for the patient
From 18 Years
All Gender
Medical requirements
Inclusion criteria
Have liver fat content ≥8%.
Have ELF score of ≥9 and ≤10.8 at screening.
Have VCTE LSM ≥10 kilopascal (kPa) and <20 kPa at screening.
Exclusion criteria
Have any other type of liver disease other than MASLD.
Have a body mass index (BMI) <25 kilogram per square meter (kg/m2).
Prior decompensated liver disease (history of esophageal/gastric varices, ascites, hepatic encephalopathy).
Have lost more than 11 pounds within the 3 months prior to screening.
Have a hemoglobin A1c (HbA1c) greater than 10%.
Have type 1 diabetes.
Sites
CIPREC Centro de Investigación y Prevención Cardiovascular - CABA
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Av. Pueyrredón 1746 2° A, C1119 Cdad. Autónoma de Buenos Aires, Argentina
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Centro Médico Viamonte SRL - CABA, Buenos Aires
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Av. Córdoba 2019, CABA, Buenos Aires
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Instituto de Investigaciones Clínicas Mar del Plata
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Av. Colón 3456, Mar del Plata, Buenos Aires
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CEDIMBA - DIM Clínica Privada - Buenos Aires
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Belgrano 136, Ramos Mejia, Buenos Aires.
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Centro de Investigaciones Clínicas - IESR - Rosario, Santa Fe
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España 931, Rosario, Santa Fe
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Centro Médico Maffei - CABA, Buenos Aires
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Av. Cerviño 3375, CABA, Buenos Aires
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Instituto de Investigaciones Clínicas Córdoba
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Dean Funes 1161, Córdoba
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Consultorio de Investigación Clínica EMO SRL
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Eduardo Acevedo 42 1d, C1405BUB Cdad. Autónoma de Buenos Aires, Argentina
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INECO Neurociencias Oroño - Rosario
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Bv. Oroño 1508, Rosario, Santa Fe
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Centro de Diagnóstico y Rehabilitación - CEDIR
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SAN MARTIN 3169 – Santa Fe, Santa Fe. CP 3000
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Contact us
Contact us
Sponsor
Eli Lilly and Company
Study type
Interventional
Conditions
Hepatic Steatosis
Requirements
From 18 Years
All Gender
Unique study ID
clinicaltrials.gov
NCT07165028
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