drugset / Trial / NCT07007091

A Study to Assess the Relative Bioavailability of Risankizumab Following Subcutaneous Administrations With a Pre-Filled Syringe or an On-Body Injector in Healthy Adult Participants

NCT07007091

Phase 1 Completed 260 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

This study will assess the pharmacokinetics and relative Bioavailability of risankizumab following subcutaneous administration with an on-body injector relative to a prefilled syringe

Timeline

Start
2025-06-12
Primary completion
2026-01-15
Completion
2026-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.