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Recruiting Phase 3 NCT05624450

Efficacy and Safety of Tozorakimab in Patients Hospitalised for Viral Lung Infection Requiring Supplemental Oxygen

Phase 3 – large-scale trial before approval
Conditions: Viral Lung Infection and Acute Respiratory Failure

Sponsor: AstraZeneca

trial.available_in: БГ
Overview
The purpose of this study is to evaluate the effect of tozorakimab, as an add-on to SoC in patients with viral lung infection requiring supplemental oxygen, on the prevention of death or progression to IMV/ECMO.
Who can participate
Inclusion Criteria: * Adult participants ≥ 18 years old at the time of signing the informed consent form. * Patients hospitalised with viral lung infection. * Hypoxaemia requiring treatment with supplemental O2. Hypoxaemia is defined as: SpO2 ≤ 90% OR SpO2 ≤ 92% AND one or both of the following: Radiographic infiltrates by CXR/CT compatible with viral lung infection per investigator judgement. Use of accessory muscles of respiration or RR (respiratory rate) \> 22. \- Patient remains hypoxaemic at randomisation requiring treatment with supplemental oxygen. Exclusion Criteria: * Known fungal or parasitic lung infection, aspiration lung infection, lung abscess, or evidence of septic shock. Bacterial co-infection is allowed, unless, in the opinion of the investigator, bacterial infection defines the severity of the participant's condition. * Hypoxaemia caused primarily by extrapulmonary insult or by lung injury of non-infective aetiology. * Ongoing IMV/ECMO at randomisation.
Locations 38
Argentina (1)
Research Site
Buenos Aires
COMPLETED
Australia (1)
Research Site
Adelaide
Belgium (1)
Research Site
Kortrijk
Brazil (1)
Research Site
Belo Horizonte
WITHDRAWN
Bulgaria (1)
Research Site
Montana
WITHDRAWN
Canada (1)
Research Site
Calgary , Alberta
China (1)
Research Site
Beijing
Colombia (1)
Research Site
Bogota DC
WITHDRAWN
Czech Republic (1)
Research Site
Benešov
COMPLETED
Denmark (1)
Research Site
Aalborg
Egypt (1)
Research Site
Alexandria
WITHDRAWN
France (1)
Research Site
Amiens
Greece (1)
Research Site
Athens
Hong Kong (1)
Research Site
Hong Kong
WITHDRAWN
Hungary (1)
Research Site
Balassagyarmat
India (1)
Research Site
Ahmedabad
SUSPENDED
Israel (1)
Research Site
Afula
Italy (1)
Research Site
Arezzo
Japan (1)
Research Site
Chiba
Malaysia (1)
Research Site
Kota Kinabalu
Mexico (1)
Research Site
Aguascalientes
WITHDRAWN
Peru (1)
Research Site
Cusco
Philippines (1)
Research Site
Cebu
COMPLETED
Poland (1)
Research Site
Chrzanów
Puerto Rico (1)
Research Site
Bayamón
WITHDRAWN
Romania (1)
Research Site
Bucharest
WITHDRAWN
Saudi Arabia (1)
Research Site
Jeddah
Slovakia (1)
Research Site
Bratislava
WITHDRAWN
South Africa (1)
Research Site
Johannesburg, Soweto
TERMINATED
South Korea (1)
Research Site
Daegu
WITHDRAWN
Spain (1)
Research Site
Barcelona
COMPLETED
Sweden (1)
Research Site
Helsingborg
Taiwan (1)
Research Site
Kaohsiung City
Thailand (1)
Research Site
Bangkok
Turkey (1)
Research Site
Ankara
United Kingdom (1)
Research Site
Bristol
United States (1)
Research Site
Mobile , Alabama
Vietnam (1)
Research Site
Haiphong
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
13.12.2022
Completion date
19.06.2026
Registry ID
NCT05624450
Source
anzctr
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