A Study of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies
Running, not enrolling · Phase 1
Conditions studied: Advanced Cancer
In brief
The primary purpose of this study is to assess the safety and tolerability of AB801 in participants with advanced malignancies, and to determine a recommended AB801 dose for expansion.
Key facts
- Study ID
- NCT06120075
- Run by
- Arcus Biosciences, Inc.
- People needed
- 91
- Starts
- 2024-01-19
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-07-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Research Site — Denver, Colorado, United States
- Research Site — Washington D.C., District of Columbia, United States
- Research Site — Atlanta, Georgia, United States
- Research Site — Grand Rapids, Michigan, United States
- Research Site — New York, New York, United States
- Research Site — Philadelphia, Pennsylvania, United States
- Research Site — Dallas, Texas, United States
- Research Site — San Antonio, Texas, United States
- Research Site — West Valley City, Utah, United States
- Research Site — Fairfax, Virginia, United States
Full record on ClinicalTrials.gov
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