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Trials / Completed

CompletedNCT07013760

Characterize and Assess Clinical Outcomes of Patients Receiving Tezepelumab After Marketing Approval in Spain

Observational Retrospective Study to Characterize and Assess Clinical Outcomes of Patients Receiving Tezepelumab After Marketing Approval in Spain

Status
Completed
Phase
Study type
Observational
Enrollment
420 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
12 Years – 105 Years
Healthy volunteers
Not accepted

Summary

Observational retrospective study to characterize and assess clinical outcomes of patients receiving tezepelumab after marketing approval in Spain

Detailed description

T-ROSS-II has been designed to conduct a new observational study to generate additional evidence on the use of tezepelumab in severe asthma patients in routine clinical practice in Spain after its launch. This is an observational, multi-centre, retrospective, single-arm study in patients 12 years and older with severe asthma. Approximately 400 patients meeting the study eligibility criteria will be included in the T-ROSS-II.

Conditions

Timeline

Start date
2025-06-23
Primary completion
2025-12-19
Completion
2025-12-19
First posted
2025-06-10
Last updated
2026-01-12

Locations

12 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT07013760. Inclusion in this directory is not an endorsement.

Characterize and Assess Clinical Outcomes of Patients Receiving Tezepelumab After Marketing Approval in Spain (NCT07013760) · Clinical Trials Directory