drugset / Trial / NCT03968978
Tezepelumab Home Use Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tezepelumab | Monoclonal antibody | 210 mg | Subcutaneous |