drugset / Trial / NCT06753955

Phase 1 Study of ART5803 Safety and PK After IVIG in Healthy Participants

NCT06753955

Phase 1 Completed 7 enrolled Arialys Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of ART5803 following IVIG administration in healthy participants to investigate the potential interactions between ART5803 and IVIG

Timeline

Start
2025-02-25
Primary completion
2025-07-02
Completion
2025-08-19

Drugs

EvaluationDrugModalityDoseRoute
Subject ART5803 Protein / enzyme biologic Intravenous
Background Immune Globulin Intravenous (Human) Protein / enzyme biologic Intravenous