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Clinical Trials in the USA / NCT07850063
Starting soon Phase 3

ELEVATE-LIVER: A Study to Test Whether Survodutide Helps Improve Heart Structure and Function in People With Overweight or Obesity and Fatty Liver Disease

NCT07850063 · tracked via the Priya Life Science USA tracker
Phase
Phase 3
Started
2026-10-23
Last updated
2026-09-30

Condition(s) studied

ObesityMetabolic Dysfunction-associated Steatotic Liver Disease

Investigational drug(s) / intervention(s)

SurvodutidePlacebo matching survodutide

Survodutide: Survodutide

Placebo matching survodutide: Placebo matching survodutide

Study summary

This study is for adults aged 18 years and older who have a type of fatty liver disease called metabolic dysfunction-associated steatotic liver disease (MASLD). People can take part if their body mass index (BMI) is 27 kg/m² or higher, and they have certain heart and blood vessel risk factors. The purpose of this study is to find out how a medicine called survodutide affects heart structure and function in people with MASLD.

Participants are put into 2 groups randomly, which means by chance. One group gets survodutide as an injection under the skin of the abdomen once a week. The other group gets placebo as an injection once a week. Placebo looks like survodutide but does not contain any medicine. The first injection is given at the study site. Later injections are usually given by the participants themselves at home using pre-filled syringes. Participants and doctors do not know who is getting survodutide or placebo.

Participants are in the study for up to 1.5 years. During this time, they visit the study site about 14 times and have about 4 phone calls with the study staff. At some of the visits, doctors use ultrasound scans to check the heart. The results are compared between the 2 groups to see if survodutide helps improve the health of the heart. The study staff also regularly check participants' health and take note of any health problems.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key inclusion criteria: 1. Age ≥18 years at the time of signing informed consent, and at least the legal age of consent in countries where it is \>18 years 2. Signed and dated written informed consent in accordance with international council for harmonisation - good clinical practice (ICH-GCP) and local legislation prior to admission to the trial 3. Body mass index (BMI) ≥27 kg/m² 4. Hepatic steatosis established by imaging (ultrasound or cross sectional), transient elastography, or liver biopsy Further inclusion criteria apply. Key exclusion criteria: 1. Medications for obesity within 3 months before screening 2. Known or suspected hypersensitivity to the investigational medicinal product (IMP) or related products 3. Established diagnosis of heart failure or a known history of heart failure 4. Impaired renal function at screening or requiring dialysis Further exclusion criteria apply.

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
The Institute for Liver Health II DBA Arizona Clinical Trials Peoria Arizona
Cedars-Sinai Medical Center Los Angeles California
Fomat Medical Research Oxnard California
Covenant Metabolic Specialists, LLC - University Park University Park Florida
Kansas Medical Clinic PA Topeka Kansas
Southwest Gastroenterology Associates, P.C. Albuquerque New Mexico
Duke University Medical Center Durham North Carolina
Zhongshan Hospital Affiliated to Fudan University Shanghai China
Universitätsklinikum Freiburg Freiburg im Breisgau Germany
Ascires Valencia Spain
Leicester Royal Infirmary Leicester United Kingdom

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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 NCT07850063 on ClinicalTrials.gov ↗ ← All trials in the USA