drugset / Trial / NCT06968338

A Study to Assess the Safety of ARGX-213 in Healthy Volunteers

NCT06968338 ↗

Phase 1 Completed 88 enrolled argenx
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study aims to assess the safety of ARGX-213 in healthy adults. Another aim is to measure the amount of ARGX-213 in the blood over time to learn how it moves through the body and acts in the body. The participants will remain in the study for approximately up to 21 weeks.

Timeline

Start
2025-04-11
Primary completion
2026-03-20
Completion
2026-03-20

Drugs

EvaluationDrugModalityDoseRoute
Subject ARGX-213 Unknown — Intravenous

Indications

No indication recorded.