drugset / Trial / NCT03968978

Tezepelumab Home Use Study

NCT03968978

Phase 3 Completed 216 enrolled AstraZeneca Amgen · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, randomized, open-label, parallel-group study designed to assess healthcare provider and subject/caregiver reported functionality and performance of a single-use accessorized pre-filled syringe (APFS) or autoinjector (AI) with a fixed 210 mg dose of tezepelumab administered subcutaneously in the clinic and in an at-home setting.

Timeline

Start
2019-05-21
Primary completion
2020-06-05
Completion
2020-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody 210 mg Subcutaneous

Indications