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Completed Phase 2 Interventional Results available

An Efficacy and Safety Study of Mitiperstat (AZD4831) (MPO Inhibitor) vs Placebo in the Treatment of Moderate to Severe COPD.

ClinicalTrials.gov ID: NCT05492877

Public ClinicalTrials.gov record NCT05492877. 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 Oct 28, 2026, 6:20 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 IIa Randomised, Double Blind, Placebo Controlled, Parallel Arm, Multi-Centre Study to Evaluate the Efficacy and Safety of Mitiperstat (AZD4831), for 12-24 Weeks, in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a research study to evaluate the efficacy and safety of the investigational drug Mitiperstat (AZD4831) in adult patients with chronic obstructive pulmonary disease.

Study identification

NCT ID
NCT05492877
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
381 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 80 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
Nov 14, 2022 (Actual)
Primary completion
Aug 12, 2024 (Actual)
Completion
Aug 12, 2024 (Actual)
Last update posted
Aug 29, 2025

2022 – 2024

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Research Site Newport Beach California 92663 —
Research Site Clearwater Florida 33765 —
Research Site DeLand Florida 32720 —
Research Site Miami Florida 33186 —
Research Site Orlando Florida 32825 —
Research Site Tampa Florida 33606 —
Research Site Winter Park Florida 32789 —
Research Site Chicago Ridge Illinois 60415 —
Research Site Ann Arbor Michigan 48109 —
Research Site Chesterfield Missouri 63017 —
Research Site Saint Charles Missouri 63301 —
Research Site New Windsor New York 12553 —
Research Site Gastonia North Carolina 28054 —
Research Site Kernersville North Carolina 27284 —
Research Site New Bern North Carolina 28562 —
Research Site Columbus Ohio 43215 —
Research Site Choctaw Oklahoma 73020 —
Research Site Fort Mill South Carolina 29707 —
Research Site Amarillo Texas 79106 —

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 82 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05492877, 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 Aug 29, 2025 · Synced Oct 28, 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 public registry record, listed eligibility criteria, and available contact information for NCT05492877 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →