This is a Phase 2, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of pemvidutide in subjects with ALD. * Pemvidutide: 2.4 mg SC once weekly * Placebo: Placebo SC once weekly
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
100
Pemvidutide 2.4 mg
Subcutaneous injection
Relative (%) change in liver stiffness by VCTE compared to baseline at Week 24
Time frame: Week 24
Relative (%) change in liver stiffness by VCTE compared to baseline at Week 48
Time frame: Week 24 and 48
Absolute change in the Enhanced Liver Fibrosis (ELF) score at Weeks 24 and 48 compared to baseline
Time frame: Week 24 and 48
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Altimmune Clinical Study Site
Peoria, Arizona, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Tucson, Arizona, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
North Little Rock, Arkansas, United States
RECRUITINGAltimmune Clinical Study Site
Fresno, California, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
La Jolla, California, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Pasadena, California, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Englewood, Colorado, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Bradenton, Florida, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Doral, Florida, United States
NOT_YET_RECRUITINGAltimmune Clinical Study Site
Doral, Florida, United States
RECRUITING...and 25 more locations