drugset / Trial / NCT05940402

A Study to Evaluate Pharmacokinetic and Safety Trial of Emraclidine in Participants With Renal Impairment Compared With Participants With Normal Renal Function

NCT05940402

Phase 1 Completed 58 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary purpose of this study is to assess the effect of renal impairment on the pharmacokinetics (PK) of emraclidine following administration of a single oral dose in participants with mild, moderate, and severe renal impairment relative to matched participants with normal renal function.

Timeline

Start
2023-07-24
Primary completion
2024-12-19
Completion
2024-12-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Emraclidine Small molecule 10 mg Oral