drugset / Trial / NCT06004921

A Study to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of AB801 in Healthy Volunteers

NCT06004921

Phase 1 Completed 32 enrolled Arcus Biosciences, Inc.
RandomizedSequentialDouble-blindTreatment

Summary

The primary purpose of this study is to determine the safety and tolerability of AB801, and to understand the pharmacokinetic (PK) profile of AB801 when taken as a capsule and tablet in healthy volunteers.

Timeline

Start
2023-10-16
Primary completion
2024-02-23
Completion
2024-02-23

Drugs

EvaluationDrugModalityDoseRoute
Subject AB801 Unknown

Indications