Efficacy and Safety of Tozorakimab in Patients Hospitalised for Viral Lung Infection Requiring Supplemental Oxygen
AstraZeneca · NCT05624450
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 3527
- US sites recruiting
- 31
- Study start
- December 13, 2022
- Record last updated
- October 2, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Tozorakimab; Placebo
Conditions: Viral Lung Infection and Acute Respiratory Failure
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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.
Recruiting US locations
Research Site
Mobile, AL 36608
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Tucson, AZ 85719
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Fresno, CA 93701
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Newport Beach, CA 92663
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Torrance, CA 90505
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Colorado Springs, CO 80909
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Washington D.C., DC 20037
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Gainesville, FL 32611
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Jacksonville, FL 32224
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Lakeland, FL 33805
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Tampa, FL 33617
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Boise, ID 83702
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Evanston, IL 60201
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Louisville, KY 40202
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Baton Rouge, LA 70808
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Annapolis, MD 21401
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Detroit, MI 48202
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Royal Oak, MI 48073
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Saint Paul, MN 55101
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Kansas City, MO 64108
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St Louis, MO 63110
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New York, NY 10039
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Winston-Salem, NC 27157
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Columbus, OH 43210
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Toledo, OH 43614
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Oklahoma City, OK 73104
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Greenville, SC 29605
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Dallas, TX 75204
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El Paso, TX 79905
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Salt Lake City, UT 84107
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Charlottesville, VA 22908
Study contacts (from the official record)
- AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com