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Help ENLIGHTEN MASH/NASH treatment options.

Together, let’s find a treatment for MASH/NASH to reduce the worsening of cirrhosis and development of complications of cirrhosis. Consider joining the ENLIGHTEN Cirrhosis study, which is researching the investigational drug, pegozafermin.  

Study Clinic Locations

Help ENLIGHTEN MASH/NASH treatment options.

Together, let’s find a treatment for MASH/NASH to reduce the worsening of cirrhosis and development of complications of cirrhosis. Consider joining the ENLIGHTEN Cirrhosis study, which is researching the investigational drug, pegozafermin.  

Study Clinic Locations

About MASH/NASH Cirrhosis

What is MASH/NASH?

MASH, or Metabolic Dysfunction-Associated Steatohepatitis, is a chronic liver disease. MASH is caused by the buildup of fat in the liver leading to inflammation and damage. If left untreated, MASH can cause scarring (fibrosis) and eventually cirrhosis can occur.

MASH is an advanced form of the common MASLD, metabolic dysfunction-associated steatotic liver disease. About 20% of people with MASLD develop MASH. It is most common in people who are obese and/or have Type 2 diabetes. Cirrhosis is a late-stage condition characterized by the irreversible scarring (fibrosis) of the liver due to long-term, continuous damage. This progressive disease replaces healthy liver tissue with scar tissue, which obstructs the liver's ability to function properly.

MASH was previously known as NASH, or Nonalcoholic Steatohepatitis. In an effort to destigmatize the disease, researchers and medical professionals agree that MASH is a more accurate description. This name drives the focus to the metabolic origins of the disease rather than the nonalcoholic component.

During this time of transition between names, both NASH and MASH are acceptable and can be used interchangeably.

There is currently no approved treatment or therapy for MASH or MASLD but studies like ENLIGHTEN Cirrhosis are working to change that.

What is the ENLIGHTEN Cirrhosis study?

The ENLIGHTEN Cirrhosis study is a phase 3 clinical trial for people with fatty liver disease, otherwise known as MASH/NASH, studying the effectiveness and safety of the study medication, pegozafermin. This study is for people  aged 18-75 who have been confirmed to have MASH/NASH with cirrhosis. Together, we aim to provide a potential treatment and reduce the risk of cirrhosis worsening.

How do I know if I can join the ENLIGHTEN Cirrhosis study?

You may be able to join the study if you meet the following requirements:

Age 18-75

Willing to undergo a biopsy of the liver to confirm MASH/NASH cirrhosis at screening and again after 2 years of treatment

Diagnosed with compensated cirrhosis due to MASH/NASH

Other study requirements will apply.

If you do not know whether you have compensated cirrhosis due to MASH, the study doctor can help you find out.

What will happen during the study?

Participation in the ENLIGHTEN Cirrhosis study will last a minimum of 60 months (about 5 years) . Here is what you can expect if you enroll in the ENLIGHTEN Cirrhosis study:

Review & Sign the Informed Consent Form
The Informed Consent Form (ICF) contains information about the study including its goals, duration, benefits, risks, tests, and procedures.
Screening Period
(about 12 weeks)
Receive study health assessments to confirm if you qualify for the study.
The final step of screening will consist of a liver biopsy that will be used to qualify for the study and as the baseline prior to study treatment. After qualification by biopsy has been confirmed, the final step of screening is to perform an endoscopy to understand the severity of disease and final confirmation of eligibility.
Research Medication Period (about 5 years)
  • You will be assigned at random to receive either pegozafermin or a placebo (no active medication)
  • You will receive weekly injections of pegozafermin or placebo into your belly (first given by a nurse at the study clinic and then given by yourself or a caregiver at home).
  • You will have study health checks about every 2 to 3 months for the first year, then alternate phone calls and visits every 3 months for 4 more years
  • You will follow instructions for diet, activity level, and alcohol use throughout the study
Follow-up Period (4 weeks)
Visit the study clinic 4 weeks after you stop taking pegozafermin or placebo for study health checks.
Review & Sign the Informed Consent Form
The Informed Consent Form (ICF) contains information about the study including its goals, duration, benefits, risks, tests, and procedures.
Screening Period
(about 12 weeks)
Receive study health assessments to confirm if you qualify for the study.
The final step of screening will consist of a liver biopsy that will be used to qualify for the study and as the baseline prior to study treatment. After qualification by biopsy has been confirmed, the final step of screening is to perform an endoscopy to understand the severity of disease and final confirmation of eligibility.
Research Medication Period (about 5 years)
  • You will be assigned at random to receive either pegozafermin or a placebo (no active medication)
  • You will receive weekly injections of pegozafermin or placebo into your belly (first given by a nurse at the study clinic and then given by yourself or a caregiver at home).
  • You will have study health checks about every 2 to 3 months for the first year, then alternate phone calls and visits every 3 months for 4 more years
  • You will follow instructions for diet, activity level, and alcohol use throughout the study
Follow-up Period
(4 weeks)
Visit the study clinic 4 weeks after you stop taking pegozafermin or placebo for study health checks.

Participation in a clinical study is voluntary. You can ask any questions you have and may leave the study at any time, for any reason.

Travel  reimbursement may be available for participating in the study.

Want to be a part of the ENLIGHTEN Cirrhosis study?

Find a study clinic near you

Study Clinic Locations

About Pegozafermin

What is Pegozafermin?

Pegozafermin is a research medication being developed to potentially decrease the inflammation and scarring of the liver that is caused by MASH/NASH. It is a lab-made version of a hormone that the body naturally produces to help process and store fats and sugars in the blood and organs. Researchers believe that pegozafermin may help the body manage fats and sugars better so less fat builds up in the liver.

Pegozafermin is investigational. This means that it is not approved by any health or regulatory agencies. It can only be used in clinical research.

Will I receive the study drug?

If you join the study, you will be assigned at random to a group that receives pegozafermin or to a group that receives placebo. Placebo looks like pegozafermin but has no active drug, so researchers can compare results across groups.
You will have a 1 in 2  chance of being assigned to pegozafermin, neither you nor your study doctor will know your assignment.  

Participants will be placed at random in 1 of 2 groups:

  • Receive pegozafermin dose weekly
  • Receive placebo dose weekly

What is a “research medication?”

Investigational means the study medication is not approved by regulatory authorities like the US Food and Drug Administration (FDA), and it can only be used in clinical research studies like ENLIGHTEN Cirrhosis.

For more information on MASH/NASH and the name change, check out:

NEJMAASLDFatty Liver AllianceCleveland ClinicNational Institute of Health

Overview of Clinical Trials

Here are some common questions and answers about study participation.

If you have additional questions about participating in a clinical research study, contact a study clinic near you/talk to your doctor for additional information.

Study Clinic Locations

Find a study clinic near you!

Use the filters, map, and listing to find the study clinic closest to you. Contact the study clinic to learn more.

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