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Completed Phase 2 Interventional Results available

A Study to Evaluate the Safety and Efficacy of Cotadutide Given by Subcutaneous Injection in Adult Participants With Non-cirrhotic Non-alcoholic Steatohepatitis With Fibrosis

ClinicalTrials.gov ID: NCT05364931

Public ClinicalTrials.gov record NCT05364931. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 12:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Randomized, Double-blind, Placebo-controlled, Proof-of-Concept Study to Evaluate the Safety and Efficacy of Cotadutide in Participants With Non-cirrhotic Non-alcoholic Steatohepatitis With Fibrosis

Study identification

NCT ID
NCT05364931
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
54 participants

Conditions and interventions

Interventions

  • Cotadutide Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 13, 2022
Primary completion
Apr 18, 2024
Completion
Apr 18, 2024
Last update posted
Sep 2, 2025

2022 – 2024

United States locations

U.S. sites
29
U.S. states
13
U.S. cities
26
Facility City State ZIP Site status
Research Site Tucson Arizona 85712
Research Site Canoga Park California 91303
Research Site Gilroy California 95020
Research Site Sacramento California 95821
Research Site Englewood Colorado 80113
Research Site Bradenton Florida 34208
Research Site Homestead Florida 33032
Research Site Jacksonville Florida 32216
Research Site Miami Florida 33175
Research Site Miami Florida 33176
Research Site Winter Park Florida 32789
Research Site Munster Indiana 46321
Research Site Houma Louisiana 70363
Research Site Marrero Louisiana 70006
Research Site Marrero Louisiana 70072
Research Site Shreveport Louisiana 71105
Research Site Ann Arbor Michigan 48109
Research Site Las Vegas Nevada 89104
Research Site Las Vegas Nevada 89109
Research Site Lawrence New Jersey 08648
Research Site Warren Township New Jersey 07059
Research Site Morehead City North Carolina 28557
Research Site Chattanooga Tennessee 37421
Research Site Arlington Texas 76012
Research Site Austin Texas 78745
Research Site Dallas Texas 75230
Research Site Lewisville Texas 75057
Research Site San Antonio Texas 78215
Research Site Ogden Utah 84403

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 86 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05364931, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 2, 2025 · Synced Jul 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05364931 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →