Patient Guide: A Study Evaluating Efruxifermin in Subjects With Non-invasively Diagnosed Nonalcoholic Steatohepatitis (NASH)/Metabolic Dysfunction-Associated Steatohepatitis (MASH) and Nonalcoholic Fatty Liver Disease (NAFLD)/Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 211 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06161571
Status: ACTIVE_NOT_RECRUITING
Condition: NASH/MASH, NAFLD/MASLD
Phase: PHASE3

Where You Can Participate

This study is available at 211 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Chandler, Arizona
  • • Flagstaff, Arizona
  • • And 208 more locations

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A Study Evaluating Efruxifermin in Subjects With Non-invasively Diagnosed Nonalcoholic Steatohepatitis (NASH)/Metabolic Dysfunction-Associated Steatohepatitis (MASH) and Nonalcoholic Fatty Liver Disease (NAFLD)/Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) - Join Clinical Trial NCTNCT06161571

How to Join This Clinical Trial - NCTNCT06161571

Learn how to participate in this PHASE3 trial studying an investigational therapy for NASH/MASH, NAFLD/MASLD. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with NASH/MASH, NAFLD/MASLD. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
NASH/MASH, NAFLD/MASLD
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06161571 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 211 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35209 - United States

Status: Contact for availability

Clinical Research Site

Chandler, Arizona 85224 - United States

Status: Contact for availability

Clinical Research Site

Flagstaff, Arizona 86001 - United States

Status: Contact for availability

Clinical Research Site

Peoria, Arizona 85381 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85712 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85715 - United States

Status: Contact for availability

Clinical Research Site

Conway, Arkansas 72032 - United States

Status: Contact for availability

Clinical Research Site

Jonesboro, Arkansas 72401 - United States

Status: Contact for availability

Clinical Research Site

Little Rock, Arkansas 72205 - United States

Status: Contact for availability

Clinical Research Site

North Little Rock, Arkansas 72117 - United States

Status: Contact for availability

And 201 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for NASH/MASH, NAFLD/MASLD:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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