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ACTIVE NOT RECRUITING
NCT05039450
PHASE2

A Study of Efruxifermin in Subjects With Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis (NASH) (Symmetry)

Sponsor: Akero Therapeutics, Inc

View on ClinicalTrials.gov

Summary

This is a multi-center evaluation of efruxifermin (EFX) in a randomized, double-blind, placebo-controlled study in cirrhotic subjects with biopsy-proven F4 compensated NASH.

Official title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety and Efficacy of Efruxifermin in Subjects With Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis (NASH)

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

182

Start Date

2021-07-30

Completion Date

2025-05

Last Updated

2025-04-09

Healthy Volunteers

No

Interventions

DRUG

EFX

Investigational drug, Efruxifermin

DRUG

Placebo

Placebo

Locations (49)

Akero Clinical Study Site

Chandler, Arizona, United States

Akero Clinical Study Site

Glendale, Arizona, United States

Akero Clinical Study Site

Tucson, Arizona, United States

Akero Clinical Study Site

Tucson, Arizona, United States

Akero Clinical Study Site

North Little Rock, Arkansas, United States

Akero Clinical Study Site

Fresno, California, United States

Akero Clinical Study Site

Long Beach, California, United States

Akero Clinical Study Site

Los Angeles, California, United States

Akero Clinical Study Site

Pasadena, California, United States

Akero Clinical Study Site

Englewood, Colorado, United States

Akero Clinical Study Site

Clearwater, Florida, United States

Akero Clinical Study Site

Fort Myers, Florida, United States

Akero Clinical Study Site

Fort Myers, Florida, United States

Akero Clinical Study Site

Hialeah Gardens, Florida, United States

Akero Clinical Study Site

Lakewood Rch, Florida, United States

Akero Clinical Study Site

Miami Lakes, Florida, United States

Akero Clinical Study Site

Ocala, Florida, United States

Akero Clinical Study Site

Sarasota, Florida, United States

Akero Clinical Study Site

South Bend, Indiana, United States

Akero Clinical Study Site

Topeka, Kansas, United States

Akero Clinical Study Site

Bastrop, Louisiana, United States

Akero Clinical Study Site

Marrero, Louisiana, United States

Akero Clinical Study Site

Las Vegas, Nevada, United States

Akero Clinical Study Site

Concord, North Carolina, United States

Akero Clinical Study Site

Fayetteville, North Carolina, United States

Akero Clinical Study Site

Morehead City, North Carolina, United States

Akero Clinical Study Site

Springboro, Ohio, United States

Akero Clinical Study Site

Westlake, Ohio, United States

Akero Clinical Study Site

Greenville, South Carolina, United States

Akero Clinical Study Site

Greenwood, South Carolina, United States

Akero Clinical Study Site

Summerville, South Carolina, United States

Akero Clinical Study Site

Nashville, Tennessee, United States

Akero Clinical Study Site

Austin, Texas, United States

Akero Clinical Study Site

Dallas, Texas, United States

Akero Clinical Study Site

Edinburg, Texas, United States

Akero Clinical Study Site

Edinburg, Texas, United States

Akero Clinical Study Site

Fort Worth, Texas, United States

Akero Clinical Study Site

Fort Worth, Texas, United States

Akero Clinical Study Site

Houston, Texas, United States

Akero Clinical Study Site

Houston, Texas, United States

Akero Clinical Study Site

San Antonio, Texas, United States

Akero Clinical Study Site

Waco, Texas, United States

Akero Clinical Study Site

Webster, Texas, United States

Akero Clinical Study Site

Wichita Falls, Texas, United States

Akero Clinical Study Site

Ogden, Utah, United States

Akero Clinical Study Site

Richmond, Virginia, United States

Akero Clinical Study Site

Mexico City, Mexico

Akero Clinical Study Site

Monterrey, Mexico

Akero Clinical Study Site

San Juan, Puerto Rico