Phase
Condition
Asthma
Treatment
Tezepelumab
Placebo
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
General
Able and willing to provide written informed consent.
Able and willing to comply with the study protocol.
Males and females ≥ 18 years of age.
Asthma-related
Asthma diagnosed by a respiratory physician ≥12 months prior to study enrolmentbased on the Global Initiative for Asthma (GINA) 2021 guidelines.
ACQ ≥1.5 at screening.
Methacholine PC20 ≤ 4 mg/mL OR ≥15% decrease in FEV1 during saline inhalationfor sputum induction OR ≥15% improvement in FEV1 after bronchodilator duringthe screening period.
Criteria met for moderate or severe asthma defined by GINA 2021 guidelines,i.e. treatment with low, medium or high dose ICS (<250 mcg, 251 - 500 mcg, >500mcg of fluticasone equivalent/day respectively) plus another controller.Patients on prednisone would not be excluded, as long as they meet the rest ofthe inclusion criteria.
FeNO >25 ppb OR ≥3% sputum eosinophils (preferred) OR blood eos ≥300/µL duringthe screening period.
History of ≥1 exacerbation in the previous year.
Exclusion
Exclusion Criteria:
- General
-- Participation in any clinical trial of an investigational agent or procedurewithin six months prior to screening or during the study.
Medical conditions and treatment history
History of anaphylaxis to any previous biologic therapy received.
Receipt of live attenuated vaccine within 30 days, receipt of COVID vaccinewithin 28 days, known or suspected COVID infection at the time of enrollment.
Acute or chronic parasitic, bacterial, fungal or viral infections thatrequired, or currently requires, hospitalization or antimicrobial treatmentduring the last four weeks.
Acute asthma exacerbation event treated with increased doses of oral, or anydose of intramuscular (IM) or intravenous (IV) corticosteroids within six weeksprior to screening.
Other relevant pulmonary diseases (e.g. chronic obstructive pulmonary disease,idiopathic pulmonary fibrosis, cystic fibrosis, pulmonary arterialhypertension, tuberculosis) requiring treatment within 12 months prior toscreening.
Alcohol or substance abuse within 12 months prior to screening.
Current smoker defined as having smoked at least one cigarette (or pipe, cigar, ormarijuana) per day for ≥ 30 days within the three months prior to screening.
Ex-smokers with ≥ 10 pack-year smoking history.
Pregnancy.
Treatment with anti-IgE, anti-IL-4, anti-IL-5, or anti-IL-13 targeted therapycurrently or within three months prior to screening.
MRI-related
Patient has an implanted mechanically, electrically or magnetically activateddevice or any metal in their body which cannot be removed, including but notlimited to pacemakers, neurostimulators, biostimulators, implanted insulinpumps, aneurysm clips, bioprosthesis, artificial limb, metallic fragment orforeign body, shunt, surgical staples (including clips or metallic suturesand/or ear implants) (at the discretion of the MRI Technologist).
In the investigator's opinion, subject suffers from any physical, psychologicalor other condition(s) that might prevent performance of the MRI, such as severeclaustrophobia.
Study Design
Study Description
Connect with a study center
Firestone Institute for Respiratory Health
Hamilton, Ontario L8N 4A6
CanadaSite Not Available
Firestone Institute for Respiratory Health
Hamilton 5969782, Ontario 6093943 L8N 4A6
CanadaSite Not Available

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