drugset / Trial / NCT05305222

A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokinetics, Safety and Tolerability of Risankizumab

NCT05305222

Phase 1 Completed 17 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindBasic science

Summary

The main objective of this study is to assess the pharmacokinetics, safety, tolerability and immunogenicity following a single intravenous (IV) infusion of risankizumab in healthy Japanese and Caucasian participants.

Timeline

Start
2017-10-23
Primary completion
2018-06-15
Completion
2018-06-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Intravenous

Indications

No indication recorded.