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Help ENLIGHTEN MASH/NASH treatment options.

Together, let’s find a treatment for MASH/NASH. Consider joining the ENLIGHTEN Fibrosis study, which is researching the investigational drug, pegozafermin.

Study Clinic Locations

Help ENLIGHTEN MASH/NASH treatments.

Together, let’s find a treatment for MASH/NASH. Consider joining the ENLIGHTEN Fibrosis study, which is researching the investigational drug, pegozafermin.

Study Clinic Locations

About MASH/NASH Fibrosis

What is MASH/NASH Fibrosis?

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. 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.

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 are currently very few approved treatments or therapies for MASH or MASLD but studies like ENLIGHTEN Fibrosis are working to change that.

What is the ENLIGHTEN Fibrosis study?

The ENLIGHTEN Fibrosis 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 fibrosis. Together, we aim to provide a potential treatment and improve the lives of people living with MASH/NASH.

How do I know if I can join the ENLIGHTEN Fibrosis 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 and again after 12 months and 36 months of treatment

Confirmed diagnosis of MASH/NASH with F2 or F3 Fibrosis

Other study requirements will apply.

What will happen during the study?

Participation in the ENLIGHTEN Fibrosis study will last a minimum of 40 months (about 3 and a half years). Here is what you can expect if you enroll in the ENLIGHTEN Fibrosis 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.
Research Medication Period (36 months with possible extension)
  • You will be assigned at random to receive either pegozafermin or a placebo (no active medication)
  • You will receive 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) either weekly or every 2 weeks, depending on your assigned schedule.
  • 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 2 more years
  • You will follow instructions for diet, activity level, and alcohol use throughout the study
Follow-up Period
(3 weeks)
Visit the study clinic 3 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.
Research Medication Period (36 months with possible extension)
  • You will be assigned at random to receive either pegozafermin or a placebo (no active medication)
  • You will receive 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) either weekly or every 2 weeks, depending on your assigned schedule.
  • 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 2 more years
  • You will follow instructions for diet, activity level, and alcohol use throughout the study
Follow-up Period
(3 weeks)
Visit the study clinic 3 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 and reimbursement may be available for participating in the study.

Want to be a part of the ENLIGHTEN Fibrosis 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 2 in 3 chance of being assigned to pegozafermin, but you will not know your assignment.

Participants will be placed at random in 1 of 4 groups:

  • Receive pegozafermin dose weekly
  • Receive pegozafermin dose once every 2 weeks
  • Receive placebo dose weekly
  • Receive placebo dose once every 2 weeks

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 Fibrosis.

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

NEJMFatty Liver AllianceCleveland ClinicNational Institute of HealthAASLD

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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