drugset / Trial / NCT06487572

A Study to Assess Pharmacokinetic Exposures Following Intravenous and Subcutaneous Administration of Risankizumab in Healthy Participants

NCT06487572

Phase 1 Completed 60 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

The objective of this study is to compare pharmacokinetic exposures following intravenous and subcutaneous administration of Risankizumab.

Timeline

Start
2024-07-23
Primary completion
2025-02-07
Completion
2025-02-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Intravenous

Indications

No indication recorded.