drugset / Trial / NCT07688980
Study to Characterise Pharmacokinetics (PK), Pharmacodynamics (PD), and Safety of Anifrolumab Administered Subcutaneously (SC) or Intravenously (IV)
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to assess the PK, PD, and safety of anifrolumab as SC administration or IV infusion in adult participants with systemic lupus erythematosus (SLE).
Timeline
- Start
- 2026-10-30
- Primary completion
- 2029-04-13
- Completion
- 2030-06-14
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Anifrolumab | Monoclonal antibody | — | Subcutaneous |