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Help Shape the Future of Liver Disease Treatment

Fatty Liver Disease

Join our ethically approved fatty liver disease clinical research trial at 4MCS and help
develop better treatments for people living with this increasingly common condition across the
UK.

Are You Eligible?

Check Your Eligibility Now

You may be eligible for our fatty liver disease clinical trial if you:

Additional eligibility criteria may apply. Our research team will discuss full eligibility requirements with you during your initial consultation.

Are aged 18 years or older

Have been diagnosed with fatty liver disease

Have at least one metabolic risk factor

Live within distance of our Ilford facility

fatty liver disease clinical trials​ in uk

Current Trials

Fatty liver disease is estimated to affect up to 1 in 5 people in the UK, making it one of the most common liver conditions. Many people do not know they have it because it often causes no symptoms in its early stages. That is why your participation in clinical research trials is so important.

Fatty Liver Disease clinical trials​

What is Fatty Liver Disease?

Fatty liver disease, also known as metabolic dysfunction-associated steatotic liver disease (MASLD), is a condition where excess fat builds up in the liver. A healthy liver should contain little or no fat. When too much fat accumulates, it can cause inflammation, scarring, and reduced liver function over time.

Fatty liver disease often has no obvious symptoms in its early stages. However, if left untreated, it can progress through several stages and may eventually lead to:

Fatty liver disease is closely linked with other metabolic conditions such as type 2 diabetes, obesity, and heart disease. If you have been diagnosed with high blood pressure, you may also be interested in our hypertension clinical trials, as these conditions often occur together and share similar risk factors.

Fatty Liver Disease clinical trials​ in uk

How does it work?

Register Your Interest

Complete our simple online form or give us a call to express your interest. We will ask you some basic questions about your liver health and any metabolic conditions you may have. This initial conversation is completely confidential and helps us understand if our current trial might be suitable for you.

Attend Your Screening Visit

If you appear eligible, we will invite you to our Ilford facility for a comprehensive screening appointment. During this visit, our experienced research team will conduct a thorough health assessment, review your medical history, and may perform tests to assess your liver function. We will check whether you meet all the specific criteria for the trial. 

Not sure what a screening visit involves? Our guide explains what happens at a clinical trial screening visit so you know exactly what to expect. We will answer all your questions and make sure you fully understand what participation involves.

Begin Your Trial Participation

Once confirmed as eligible and you have provided your informed consent, you will begin the trial. You will attend regular visits to our facility where you will receive the investigational treatment, undergo health monitoring, and complete assessments. Our dedicated team will support you throughout the entire process, ensuring your safety and comfort at every stage. 

If you would like to know more about the consent process, you can read about what informed consent means and your rights as a participant.

Fatty Liver Disease clinical trials​

Why Fatty Liver Disease Clinical Research Matters

Clinical trials are essential for developing new and improved treatments for fatty liver disease. Currently, there is no specific medication approved for treating fatty liver disease, which makes research even more important. Through fatty liver disease clinical research trials, we can:

Your participation in our fatty liver disease clinical trial could help millions of people protect their liver health and avoid serious complications. To understand more about why this research matters, read about the real value of joining a clinical trial.

Fatty Liver Disease clinical trials​

How You Can Benefit from Participating

Taking part in our fatty liver disease clinical research trial offers several potential benefits:

Medical Care and Monitoring

You will have access to specialist medical care and regular health monitoring throughout the trial. This includes detailed assessments of your liver health by experienced specialists, plus potential early access to innovative treatments not yet widely available. Our team follows strict safety protocols, which you can learn more about in our article on how clinical trials protect participants.

Contributing to Medical Progress

By taking part, you help advance liver disease research that could benefit millions of people
worldwide. You play a direct role in developing better treatments for future generations and
contribute valuable data that helps researchers understand fatty liver disease better.

Professional Support

You will receive expert guidance from our experienced clinical research team, including regular check-ups and professional medical supervision. You will also have access to educational resources about liver health management. Many participants find the experience positive, and you can read what others have said on our testimonials page.

clinical trials for fatty liver disease

Why Choose 4MCS?

You may be eligible for our fatty liver disease clinical trials if you:

Established Expertise:

4MCS is a privately owned company specialising in clinical research with a dedicated site in Ilford and Swinton in the UK, established in 2018 with extensive industry experience. 

Proven Track Record:

Our team has successfully conducted clinical trials across Phase 1b to Phase 4, contributing to medical advancements and improved patient outcomes with MASLD.

Patient-Centred Care:

We maintain a repository of over 35,000 patients with a wide range of diseases and are committed to providing personalised care throughout your trial participation. Read what our participants say.

Comprehensive Support:

From your first enquiry through to trial completion, our dedicated team provides ongoing support, ensuring you feel informed and comfortable throughout your participation. View our FAQs for answers to common questions, or read what you should know before participating in a clinical trial.

speak to an expert

Enquire to participate

Become A Participant

Fatty liver disease clinical trials​

Frequently Asked Questions

We understand you may have questions about participating in our fatty liver disease clinical trials. Here are answers to some of the most common questions we receive from potential participants.

Am I eligible to participate in a fatty liver disease clinical trial at 4MCS?

To be eligible for our fatty liver disease clinical trial, you must be aged 18 years or older and have been diagnosed with fatty liver disease. This includes non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), or fatty liver. You should also have at least one metabolic risk factor, such as type 2 diabetes, obesity, hypertension, or high cholesterol. 

During your initial consultation, we will review your medical history, current medications, and overall health. Do not worry if you are unsure whether you qualify. Our experienced team will guide you through the eligibility process and ensure you have all the information you need. For more answers to common questions, visit our frequently asked questions page.

Participating in our fatty liver disease clinical study involves regular visits to our research facility in Ilford. During these visits, you will receive comprehensive medical assessments from our qualified research team, including liver function tests, blood tests, and general health checks. Some trials may also include imaging scans to assess your liver. 

The trial process typically includes an initial screening period to confirm your eligibility, followed by the main study period where you may receive either the investigational treatment or a placebo. You can learn more about what happens at a clinical trial screening visit to help you prepare. Throughout the trial, you may be asked to keep a diary documenting any changes you experience. Our team will provide you with all the necessary information and support. Your safety and wellbeing are our absolute priority throughout the entire process, and you can read more about how clinical trials protect participants

Our clinical research facility is located in Ilford, providing easy access for participants across London and the surrounding areas. The facility is well-connected by public transport, with convenient links to central London and the wider metropolitan area. 

Our site features modern, purpose-built clinical research facilities designed to provide a comfortable and professional environment for trial participants. We have parking available for those who prefer to drive, and our friendly staff can provide detailed directions and travel information to help you plan your visits. You can also contact us directly for directions or to ask any questions about visiting our facility. 

With access to a population of over 10 million residing close to our research unit, our location enables us to conduct comprehensive fatty liver disease clinical research trials while ensuring convenient access for participants. Learn more about us and our research capabilities.

At 4MCS, we maintain the highest standards of clinical research through rigorous quality assurance processes and regulatory compliance. Our experienced team includes qualified medical professionals, research coordinators, and regulatory specialists who ensure every aspect of our fatty liver disease clinical research trial meets international standards. We follow Good Clinical Practice (GCP) guidelines and work closely with regulatory authorities to maintain compliance throughout all stages of research. 

We also maintain comprehensive safety monitoring protocols, with regular safety reviews and immediate reporting procedures for any adverse events. All trial data is handled with the utmost confidentiality and security, following strict data protection protocols. We are committed to transparency and will keep you fully informed about your trial progress and any relevant findings. To understand more about your rights during the trial, read about what informed consent means in clinical trials.