Clinical Trial

Study to Characterise Pharmacokinetics (PK), Pharmacodynamics (PD), and Safety of Anifrolumab Administered Subcutaneously (SC) or Intravenously (IV)

Not Yet Recruiting Phase 1
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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).
Trial Details
NCT Number NCT07688980
Lead Sponsor AstraZeneca
Collaborators: Parexel
Conditions Systemic Lupus Erythematosus
Enrollment 92 participants
Start Date 2026-10-30
Primary Completion 2029-04-13 (estimated)
Study Completion 2030-06-14 (estimated)
Updated on ClinicalTrials.gov 2026-07-07