drugset / Trial / NCT07856004

A Study to Investigate Safety, Tolerability, and Pharmacokinetics of Tacabrutideg (BGB-16673) in Participants With Moderate and Severe Hepatic Impairment

NCT07856004 ↗

Phase 1 Not yet recruiting 24 enrolled BeOne Medicines
Non-randomizedParallel-groupOpen-labelOther

Summary

The goal of this study is to understand how the body processes tacabrutideg in adults with different levels of liver function (normal, moderate impairment, and severe impairment).

Timeline

Start
2026-10-22
Primary completion
2027-07-31
Completion
2027-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacabrutideg Unknown — Oral

Indications

No indication recorded.