drugset / Trial / NCT07688980

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

NCT07688980

Phase 1 Not yet recruiting 92 enrolled AstraZeneca Parexel · collab
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

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody Subcutaneous