drugset / Trial / NCT06937619

A Study to Assess the Relative Bioavailability of Risankizumab Following Subcutaneous Administration With On-Body Injector in Healthy Adult Participants

NCT06937619

Phase 1 Completed 263 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

This study will assess the pharmacokinetics and relative Bioavailability of risankizumab following subcutaneous (SC) administration with on-body Injector in Healthy Adult Participants.

Timeline

Start
2025-04-21
Primary completion
2025-11-10
Completion
2025-11-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.