The primary objective of the study is to evaluate the effect of TEV-48574 compared with placebo on loss of asthma control (LoAC) in adult patients with T2-low and non-T2 severe asthma uncontrolled on inhaled corticosteroids plus long-acting beta-agonists (ICS+LABA).
The secondary efficacy objective is to evaluate the effect of TEV-48574 compared with placebo on a range of clinical measures of asthma control.
The duration of patient participation in the study is planned to be up to approximately 30 weeks.
| Condition | Asthma |
|---|---|
| Treatment | Placebo, TEV-48574 |
| Clinical Study Identifier | NCT04545385 |
| Sponsor | Teva Branded Pharmaceutical Products R&D, Inc. |
| Last Modified on | 28 April 2022 |
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