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Completed Phase 3 Interventional

Efficacy and Safety of Tozorakimab in Symptomatic Chronic Obstructive Pulmonary Disease With a History of Exacerbations

ClinicalTrials.gov ID: NCT05166889

Public ClinicalTrials.gov record NCT05166889. 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 Sep 2, 2026, 5:19 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 III, Multicentre, Randomised, Double-blind, Chronic-dosing, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Two Dose Regimens of Tozorakimab in Participants With Symptomatic Chronic Obstructive Pulmonary Disease (COPD) With a History of COPD Exacerbations (OBERON)

Brief summary

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

The purpose of this Phase III study is to evaluate the efficacy and safety of tozorakimab Dose 1 and Dose 2 administered subcutaneously (SC) in adult participants with symptomatic COPD and history of ≥ 2 moderate or ≥ 1 severe exacerbation of COPD in the previous 12 months. Participants should be receiving optimised treatment with maintenance inhaled therapy (ICS/LABA/LAMA triple therapy, or dual therapy if triple is not considered appropriate) in stable doses throughout at least 3 months prior to enrolment.

Study identification

NCT ID
NCT05166889
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,132 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 130 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
Jan 2, 2022
Primary completion
Jan 18, 2026
Completion
Mar 10, 2026
Last update posted
Apr 15, 2026

2022 – 2026

United States locations

U.S. sites
36
U.S. states
23
U.S. cities
36
Facility City State ZIP Site status
Research Site Huntsville Alabama 35801
Research Site Mobile Alabama 36608
Research Site Montgomery Alabama 36106
Research Site Phoenix Arizona 85044
Research Site Bakersfield California 93301
Research Site Sacramento California 95821
Research Site Boynton Beach Florida 33435
Research Site Ormond Beach Florida 32174
Research Site Plantation Florida 33324
Research Site Meridian Idaho 83642
Research Site Evergreen Park Illinois 60805
Research Site Normal Illinois 61761
Research Site Iowa City Iowa 52242
Research Site Kansas City Kansas 66104
Research Site Baton Rouge Louisiana 70816
Research Site Zachary Louisiana 70791
Research Site Baltimore Maryland 21224
Research Site Rochester Minnesota 55905
Research Site St Louis Missouri 63110
Research Site Missoula Montana 59808
Research Site Brick New Jersey 08724
Research Site New York New York 10037
Research Site The Bronx New York 10455
Research Site Charlotte North Carolina 28277
Research Site Durham North Carolina 27710
Research Site Gastonia North Carolina 28054
Research Site Fargo North Dakota 58104
Research Site DuBois Pennsylvania 15801
Research Site Pittsburgh Pennsylvania 15213
Research Site Sayre Pennsylvania 18840
Research Site Rapid City South Dakota 57702
Research Site Franklin Tennessee 37067
Research Site Houston Texas 77022
Research Site Kingwood Texas 77339
Research Site Salt Lake City Utah 84108
Research Site Burlington Vermont 05401

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 176 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05166889, 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 Apr 15, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05166889 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →