drugset / Trial / NCT05062759

Study to Assess the Effect of Tezepelumab on the Immune Response to Influenza Vaccination in Participants With Asthma

NCT05062759

Phase 3 Completed 70 enrolled AstraZeneca Amgen · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 3b, multicenter, randomized, double-blind, parallel group, placebo-controlled study designed to investigate the potential effect of tezepelumab (210 mg subcutaneous \[SC\] every 4 weeks \[Q4W\]) on antibody responses following seasonal quadrivalent influenza virus vaccination in the fall/winter 2021-2022 in the USA.

Timeline

Start
2021-08-23
Primary completion
2022-03-21
Completion
2022-07-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody 210 mg Subcutaneous

Indications