drugset / Trial / NCT03451422

Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Efavaleukin Alfa in Participants With Systemic Lupus Erythematosus

NCT03451422 ↗

Phase 1 Completed 35 enrolled Amgen
RandomizedParallel-groupTriple-blindBasic science

Summary

To evaluate the safety and tolerability of subcutaneous (SC) dose administrations of Efavaleukin Alfa in participants with systemic lupus erythematosus (SLE).

Timeline

Start
2018-04-10
Primary completion
2021-10-12
Completion
2021-10-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavaleukin alfa Protein / enzyme biologic — Subcutaneous