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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: NCT05158387

Public ClinicalTrials.gov record NCT05158387. 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, 6:58 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 (TITANIA)

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
NCT05158387
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,172 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
Feb 6, 2022
Primary completion
Jan 18, 2026
Completion
Mar 21, 2026
Last update posted
Apr 15, 2026

2022 – 2026

United States locations

U.S. sites
34
U.S. states
19
U.S. cities
34
Facility City State ZIP Site status
Research Site Sheffield Alabama 35660
Research Site Lincoln California 95648
Research Site Newport Beach California 92663
Research Site Northridge California 91324
Research Site Colorado Springs Colorado 80909
Research Site Newark Delaware 19713
Research Site Bay Pines Florida 33744
Research Site Cape Coral Florida 33990
Research Site Pensacola Florida 32503
Research Site Tampa Florida 33607
Research Site Winter Park Florida 32789
Research Site Macon Georgia 31201
Research Site Greenwood Indiana 46143
Research Site Bowling Green Kentucky 42101
Research Site White Marsh Maryland 21162
Research Site North Dartmouth Massachusetts 02747
Research Site Ann Arbor Michigan 48109
Research Site Farmington Hills Michigan 48336
Research Site Grand Rapids Michigan 49546
Research Site Buffalo New York 14203
Research Site The Bronx New York 10459
Research Site Toledo Ohio 43617
Research Site Oklahoma City Oklahoma 73104
Research Site Tulsa Oklahoma 74133
Research Site Philadelphia Pennsylvania 19140
Research Site Rock Hill South Carolina 29732
Research Site Amarillo Texas 79106
Research Site Boerne Texas 78006
Research Site Fort Worth Texas 76104
Research Site McKinney Texas 75069
Research Site Tomball Texas 77375
Research Site Webster Texas 77598
Research Site Williamsburg Virginia 23188
Research Site Cudahy Wisconsin 53110

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 178 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05158387, 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 NCT05158387 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →