RESTORE TRIAL: A Phase 2 Study Evaluating the Efficacy and Safety of Pemvidutide in the Treatment of Alcohol-Associated Liver Disease (ALD)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAltimmune, Inc.

About this trial

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

Eligibility criteria

Qualifiers

Male or female ages 18 to 75 years, inclusive

Overweight or obesity, defined as BMI ≥ 25 kg/m2

History of alcohol misuse for the prior 3 years, with an alcohol intake ≥ 50 grams per day for males and ≥ 40 grams per day for females on average in the past year

Liver stiffness of 10.0-18.5 kPa by VCTE, inclusive

Disqualifiers

Presence of clinically significant alcohol withdrawal symptoms, defined as CIWA-Ar score ≥ 10 at screening and/or prior to randomization

History of hospitalization for alcohol intoxication or alcohol withdrawal within the past year

History of seizures related to alcohol within the past year

History and/or current DSM-5 diagnosis of schizophrenia, bipolar disorder, psychotic disorder, or another severe psychiatric disorder, unless documented as well-controlled by the Investigator for at least 6 months prior to screening and cleared by the Medical Monitor

Trial design

Treatments tested in this trial

  • Pemvidutide
  • Placebo

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

43
Puerto Rico
Altimmune Clinical Study Site00927, San JuanPuerto Rico, Puerto Rico
United States
Arizona
Altimmune Clinical Study Site85381, Peoria United States
Altimmune Clinical Study Site85712, Tucson United States
Altimmune Clinical Study Site85712, Tuscon United States

Sponsors and collaborators

Altimmune, Inc.

Lead sponsor