drugset / Trial / NCT06054425

A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Manufactured by Two Different Processes in Healthy Adults

NCT06054425

Phase 1 Completed 48 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

The objective of this study is to assess the bioavailability of risankizumab liquid vial manufactured with the new process (CMC3) relative to the current process (CMC2).

Timeline

Start
2023-11-20
Primary completion
2024-05-06
Completion
2024-05-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Intravenous

Indications

No indication recorded.