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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06419374




Registration number
NCT06419374
Ethics application status
Date submitted
14/05/2024
Date registered
17/05/2024
Date last updated
4/04/2025

Titles & IDs
Public title
A Study to Evaluate the Efficacy and Safety of Pegozafermin in Participants With Compensated Cirrhosis Due to MASH
Scientific title
A Phase 3 Study to Evaluate the Efficacy and Safety of Pegozafermin in Subjects With Compensated Cirrhosis Due to Metabolic Dysfunction-Associated Steatohepatitis (MASH) (ENLIGHTEN-Cirrhosis)
Secondary ID [1] 0 0
BIO89-100-132
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Metabolic Dysfunction-Associated Steatohepatitis (MASH) / Nonalcoholic Steatohepatitis (NASH) With Compensated Cirrhosis 0 0
Condition category
Condition code
Oral and Gastrointestinal 0 0 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Metabolic and Endocrine 0 0 0 0
Metabolic disorders
Diet and Nutrition 0 0 0 0
Obesity
Inflammatory and Immune System 0 0 0 0
Connective tissue diseases
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - Pegozafermin
Treatment: Drugs - Placebo

Experimental: Pegozafermin -

Placebo comparator: Placebo - Matched placebo


Treatment: Other: Pegozafermin
Subcutaneous injection

Treatment: Drugs: Placebo
Subcutaneous injection
Intervention code [1] 0 0
Treatment: Other
Intervention code [2] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Proportion of Participants Achieving Fibrosis Regression
Timepoint [1] 0 0
Baseline through Month 24
Primary outcome [2] 0 0
Time to First Occurrence of Disease Progression as Measured by Composite of Protocol -Specified Clinical Events
Timepoint [2] 0 0
Baseline through Month 60
Secondary outcome [1] 0 0
Change from Baseline in Enhanced Liver Fibrosis (ELF) Score
Timepoint [1] 0 0
Baseline, Month 24 and Month 60
Secondary outcome [2] 0 0
Change from Baseline in Alanine Aminotransferase (ALT) Level
Timepoint [2] 0 0
Baseline, Month 24 and Month 60
Secondary outcome [3] 0 0
Change from Baseline in FibroScan Vibration-controlled Transient Elastography (VCTE)
Timepoint [3] 0 0
Baseline, Month 24 and Month 60
Secondary outcome [4] 0 0
Proportion of Participants who Develop Clinically Significant Portal Hypertension (CSPH)
Timepoint [4] 0 0
Baseline through Month 60

Eligibility
Key inclusion criteria
Key

* Males or non-pregnant females aged between 18 and 75 years (inclusive) at time of signing the informed consent form (ICF).
* At least 1 metabolic risk factor.
* Biopsy-confirmed fibrosis stage F4 MASH (per non-alcoholic steatohepatitis [NASH] Clinical Research Network (CRN) system) with compensated cirrhosis.
* Body mass index (BMI) at screening =25.0 (=23.0 for Asian participants) and <50.0 kilograms (kg)/meters squared (m^2).

Key
Minimum age
18 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Liver disorder other than MASH.
* History or evidence of hepatic decompensation.
* History or evidence of hepatocellular carcinoma.
* Have type 1 diabetes mellitus or poorly controlled type 2 diabetes mellitus.
* ALT or aspartate aminotransferase (AST) =250 units per liter (U/L).
* Participants taking vitamin E (>400 international units [IU]/day) must be on stable dose for at least 6 months prior to screening.

Other inclusion and exclusion criteria may apply.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
24/05/2024
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/08/2031
Actual
Sample size
Target
762
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
89bio Clinical Study Site - Adelaide
Recruitment hospital [2] 0 0
89bio Clinical Study Site - Fitzroy
Recruitment hospital [3] 0 0
89bio Clinical Study Site - Greenslopes
Recruitment hospital [4] 0 0
89bio Clinical Study Site - Heidelberg
Recruitment hospital [5] 0 0
89bio Clinical Study Site - Herston
Recruitment hospital [6] 0 0
89bio Clinical Study Site - Murdoch
Recruitment hospital [7] 0 0
89bio Clinical Study Site - South Brisbane
Recruitment postcode(s) [1] 0 0
SA 5000 - Adelaide
Recruitment postcode(s) [2] 0 0
03065 - Fitzroy
Recruitment postcode(s) [3] 0 0
04120 - Greenslopes
Recruitment postcode(s) [4] 0 0
3084 - Heidelberg
Recruitment postcode(s) [5] 0 0
Qld 4029 - Herston
Recruitment postcode(s) [6] 0 0
06150 - Murdoch
Recruitment postcode(s) [7] 0 0
04101 - South Brisbane
Recruitment outside Australia
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Arizona
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
89bio, Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Maya Margalit, MD
Address 0 0
89bio, Inc.
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
ENLIGHTEN clinical trial
Address 0 0
Country 0 0
Phone 0 0
1-415-432-9270
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT06419374