N1T-MC-MALO: A Master Protocol for a Randomized, Controlled, Clinical Trial of Multiple Pharmacologic Agents in Adult Participants With Metabolic Dysfunction-Associated Steatotic Liver Disease Who Are at Increased Risk of Developing Major Adverse Liver Outcomes (SYNERGY-Outcomes); N1T-MC-TZ01 Tirzepatide in participants with high-risk MASLD; N1T-MC-RT01 Retatrutide in participants with high-risk MASLD

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What is this study about?

This study is researching a condition called Metabolic Dysfunction-Associated Steatotic Liver Disease, which is a condition where excess fat builds up in the liver and can lead to liver scarring and damage over time. The study will test several different medications to see if they can help prevent serious liver problems from developing. The medications being studied include tirzepatide (also known by its code name LY3298176), which is given as an injection using a pre-filled pen, and retatrutide (also known as LY3437943), which is also given as an injection. Some participants will receive placebo instead of active medication. All study medications are given by injection under the skin.

The purpose of this study is to find out whether the study medications are better than placebo at reducing the occurrence of major liver-related complications. During the study, researchers will monitor participants for various liver problems including progression to cirrhosis (severe liver scarring), development of complications like varices (enlarged veins in the digestive tract), ascites (fluid buildup in the abdomen), hepatic encephalopathy (brain function problems caused by liver disease), and other serious liver conditions. The study will also track whether participants need liver transplantation or experience other serious outcomes.

Participants in this study will receive their assigned treatment over an extended period while being regularly monitored by the study team. The study requires participants to have evidence of liver fat confirmed by MRI (a type of imaging scan) and liver scarring confirmed through non-invasive tests, though a liver biopsy is not required to join the study. Throughout the study, participants will have regular check-ups and assessments to evaluate how well the treatment is working and to monitor their liver health and overall wellbeing.

1 study entry

after providing consent, you receive a study identification number and are scheduled for the first clinic visit, called the baseline visit.

2 baseline assessments and randomization

at the baseline visit, a series of assessments are performed, including medical history, physical examination, blood tests, and imaging to document your liver condition.

based on the study design, you are randomly assigned to receive either tirzepatide, retatrutide, or a matching placebo. the assignment is done by the study system and you are not involved in the choice.

3 medication training

you receive instruction on how to use a pre‑filled pen for subcutaneous injection. the training includes where to inject, how to prepare the dose, and how to record each injection.

4 initiation of study medication

you begin the study medication immediately after the baseline visit.

the medication is given as a subcutaneous injection once each week.

the specific dose is defined by the study protocol and may be adjusted during the trial according to safety and response criteria.

treatment continues for the entire study period, which lasts up to about 224 weeks from the baseline visit.

5 regular follow‑up visits

you attend clinic visits approximately every four weeks.

during each visit, blood tests, liver imaging, and physical examinations are performed to monitor your health and the effect of the medication.

the study staff review any side effects you have experienced and may adjust the dose if required.

6 ongoing self‑monitoring

you keep a diary of each weekly injection, noting the date, time, and any symptoms you notice.

you are instructed to report any serious or unexpected symptoms to the study team promptly.

7 study completion and final assessment

after approximately 224 weeks, the study reaches its planned end date.

a final set of assessments, including blood tests, imaging, and a physical exam, is performed to evaluate the overall outcome.

the study medication is discontinued, and you receive a summary of the study results and any follow‑up recommendations.

Who Can Join the Study?

  • Must have liver fat (called hepatic steatosis) that was shown on an MRI scan, which is a special type of picture of the inside of your body.
  • Must have liver scarring (called liver fibrosis) that was shown by tests that do not require a needle or surgery, known as non‑invasive tests.
  • A liver biopsy (taking a tiny piece of liver tissue) is not needed to join the study.
  • Both men and women are allowed to take part.
  • You must be in the age groups that the study includes (the trial allows participants in the age ranges coded as 3 and 4).

Who Cannot Join the Study?

  • You have any other kind of liver disease besides Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).
  • Your body mass index (BMI) is less than 25 kg/m², meaning you are below the weight range needed for the study (BMI is a measure of weight compared to height).
  • You have a history of cirrhosis (scarring of the liver) or related problems such as enlarged veins in the esophagus or stomach (esophageal/gastric varices), fluid buildup in the abdomen (ascites), brain issues caused by liver failure (hepatic encephalopathy), or a diagnosis of cirrhosis from a liver biopsy.
  • You have lost more than 11 pounds (about 5 kg) in the three months before screening.
  • Your hemoglobin A1c (HbA1c) level is greater than 10%, indicating very high average blood sugar over the past three months.
  • You have type 1 diabetes, a condition where the body does not produce insulin.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
University Multiprofile Hospital For Active Treatment And Emergency Medicine N I Pirogov Sofia Bulgaria
Universitetssykehuset Nord-Norge HF Tromsø Norway
Hopital Saint Antoine Paris France
Hopitaux Universitaires Pitie Salpetriere Paris France
Region Oestergoetland Linkoping Sweden
Universitair Ziekenhuis Gent Gent Belgium
APDP Associacao Protectora Dos Diabeticos De Portugal Lisbon Portugal
Hospital General Universitario Gregorio Maranon Madrid Spain
Hopital Beaujon Clichy France
Klinik Landstrasse Vienna Austria
Algemeen Ziekenhuis Delta Roeselare Belgium
Institutul Regional De Gastroenterologie Hepatologie Prof. Dr. Octavian Fodor Cluj Cluj Napoca Romania
Az Maria Middelares Gent Gent Belgium
Mtz Clinical Research Powered By Pratia Warsaw Poland
Delta Health Care S.R.L. Bucharest Romania
Santa Sp. z o.o. Lodz Poland
Algemeen Ziekenhuis Groeninge Kortrijk Belgium
Vitaz Sint-Niklaas Belgium
Complexo Hospitalario Universitario De Pontevedra Pontevedra Spain
Area Sanitaria De Ferrol Ferrol Spain
Centre De Recherche Clinique Portes Du Sud Venissieux France
Brain Research Center Zwolle B.V. Zwolle The Netherlands
Eugastro GmbH Leipzig Germany
Multiprofile Hospital For Active Treatment St. Ivan Rilski Gorna Oriahovitsa EOOD Gorna Oryahovitsa Bulgaria
Kresmed Sp. z o. o. Ostrow Mazowiecka Poland
Obudai Egeszseguegyi Centrum Kft. Dunaújváros Hungary
Azienda Ospedaliera di Padova Padua Italy
ID Clinic Myslowice Poland
University Of Debrecen Debrecen Hungary
Spitalul Clinic Colentina Bucuresti Bucharest Romania
Brain Research Center Den Bosch B.V. s-Hertogenbosch The Netherlands
Virgen del Rocío University Hospital Sevilla Spain
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico Milan Italy
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Universita’ Campus Bio-medico Di Roma Rome Italy
Karolinska University Hospital Solna Sweden
Stichting Radboud University Medical Center Nijmegen The Netherlands
Universitaetsklinikum Mannheim GmbH Mannheim Germany
Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz Nyiregyhaza Hungary
Spitalul Clinic Judetean De Urgenta Sfantul Apostol Andrei Constanta Constanta Romania
Pratia S.A. Skorzewo Poland
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Centre Hospitalier Universitaire De Nice Nice France
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Centre Hospitalier Universitaire Amiens Picardie Amiens France
Spital Judetean De Urgenta Satu Mare Satu Mare Romania
Centre Hospitalier Universitaire De Rennes Rennes France
Uniwersyteckie Centrum Stomatologii I Medycyny Specjalistycznej Sp. z o.o. Poznan Poland
Vrije Universiteit Brussel Jette Belgium
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo Italy
Servei De Salut De Les Illes Balears Palma Spain
Universitätsklinikum des Saarlandes – Homburg/Saar, Klinik für Urologie und Kinderurologie Homburg Germany
University Hospital Ostrava Ostrava Czechia
Krajska nemocnice Liberec a.s. Liberec Czechia
Charité Campus Virchow-Klinikum Berlin Germany
Association Hospitaliere De Bruxelles Et De Schaerbeek Centre Hospitalier Universitaire Brugmann Brussels Belgium
Mestska Nemocnice Ostrava Prispevkova Organizace Moravska Ostrava A Privoz Czechia
Universitätsmedizin Johannes Gutenberg Universität Mainz Mainz Germany
Private Practice – Dr. Lukasz Krupa Rzeszow Poland
CHU Besançon Doubs France
Centre Hospitalier Universitaire Dijon Bourgogne – Hôpital François Mitterrand Dijon France
Herz – und Diabeteszentrum Nordrhein – Westfalen, Bad Oeynhausen Bad Oeynhausen Germany
Czniurffa Urhlnaufimamen Swchdrzzt Woluwe-Saint-Lambert Belgium
Nxr Lmc Gsnfrtnvzi Tituwqjhzukjc Gttr Wiener Neustadt Austria
Cfrh Axdqze Pxelhs Sjs z oqnd Warsaw Poland
Smpgjgp Cahgbnrzcplvr Slk z oist Warsaw Poland
Ap Osnxcfri vxi Ostend Belgium
Lzinq Utbvjltwklhb Mzxsvxb Cygednb (bremj Leiden The Netherlands
Hfxvdodh Utewhcbgxxnev Maodeux Dc Vcjxaetyft Santander Spain
Csqfbqk Bgmeu Kqtvbjlvxqn Phowbcar Suw z onxu Gdansk Poland
Dwijszbg Dlibpbsz Fksphuiovmnyqbtwhjgtvw ebnp Duesseldorf Germany
Ewv Zxibjb Zamosc Poland
Ctnmtn Htajgbwcpgo Eu Utifqrdlbeuxu Dc Llzufey Limoges France
Mivnzda Ufleuvjngj Oy Gqne Graz Austria
Ezuixid Upkdmkzinwfd Mducbob Cnxzkhq Ripjjcant (tqcsncn Mte Rotterdam The Netherlands
Altyoev Otamjhsosrh Ufpalrsjbgsqr Ckbjxkwzyjpr Dtbpc Snzznb E Dqqvh Sklvnqc Dc Thtwzr Turin Italy
Aggzakojk Ujx Amsterdam The Netherlands
Ptfyjaear Ixvjehdu Mhioxzil Majhpoyzmahc Sjlrw Wqmfgrvrugwb I Ahlgduerodvfl Warsaw Poland
Grehjg Uwxphkuvws Fqabummwh Frankfurt Germany
Aiczlhq Uanqi Smexeuhlh Lyrzqd Do Bupbmix Bologna Italy
Uphwueteeu Oh Ayizmtw Edegem Belgium
Avsxdxc Oplaysipemq Ppgb Gsczulpt Xouhf Bergamo Italy
Cmeaia Hiatcpuwcwl Rqsmmmyo Dbjilakqeukwot Angers France
Fdxnwatgd Ppcu Ln Ieywctludsyqx Bmklruvhi Dop Hnvyimni Uiuqoyoaqpamv Lq Pim Madrid Spain
Hmvyejwq Uovqnzzszjukd Hysllyct Ttsvd y Pmeirs Izmqtrbm Ckgdtz dsdurzxzzitrugyta (qdss Badalona Spain
Lhwewkgswgjipypua Sgwjfqzv Salzburg Austria
Hzqqtjhn Vadu dnkzutnz Barcelona Spain
Wan Wgtlkf Iws Pcsjt Pliorwyw Khqhopo Warsaw Poland
Hzeblkeu Umxlwvzortdpv dm A Cqhlzm A Coruna Galicia Spain
Henepoxy Iepdmrk Ehxvl Huelva Spain
Ulrjoxlddqmythveszyz Rldjkyraphzexzogxl Neuruppin Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Recruiting
03.03.2026
Belgium Belgium
Recruiting
03.03.2026
Bulgaria Bulgaria
Not yet recruiting
03.03.2026
Czechia Czechia
Recruiting
03.03.2026
France France
Recruiting
03.03.2026
Germany Germany
Recruiting
03.03.2026
Hungary Hungary
Recruiting
03.03.2026
Italy Italy
Recruiting
03.03.2026
Norway Norway
Not yet recruiting
03.03.2026
Poland Poland
Recruiting
03.03.2026
Portugal Portugal
Not yet recruiting
03.03.2026
Romania Romania
Recruiting
03.03.2026
Spain Spain
Recruiting
03.03.2026
Sweden Sweden
Not yet recruiting
03.03.2026
The Netherlands The Netherlands
Not yet recruiting
03.03.2026

Trial locations

Tirzepatide is a medication that is injected under the skin using a pre‑filled pen. It works by activating hormones that help control blood sugar and can also reduce fat and inflammation in the liver. In this study, people with high‑risk metabolic dysfunction‑associated steatotic liver disease (MASLD) receive tirzepatide to find out if it lowers the chance of serious liver problems.

Retatrutide is a medication given as an injection under the skin in a liquid form. It targets similar pathways as tirzepatide and is being tested to see if it can improve liver health and lower the risk of major adverse liver outcomes in participants with high‑risk MASLD.

Metabolic Dysfunction-Associated Steatotic Liver Disease – A condition where excess fat accumulates in the liver because of metabolic problems such as obesity or diabetes. The fat buildup can cause the liver to become inflamed and swell. Over time, repeated inflammation may lead to the liver tissue becoming stiff and scarred. As scarring increases, the liver’s ability to filter blood and process nutrients can gradually decline.

Trial ID:
2025-522674-36-00
Protocol code:
N1T-MC-MALO
Trial Phase:
Therapeutic confirmatory (Phase III)

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