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Study of AB598 Monotherapy and Combination Therapy in Participants With Advanced Cancers
NCT05891171 · View on ClinicalTrials.gov ↗
Study Summary
The primary purpose of this study is to assess the safety and tolerability of AB598 in participants with advanced malignancies.
Conditions Studied
Interventions
- DRUG Fluorouracil
- DRUG Leucovorin
- DRUG Oxaliplatin
- DRUG Zimberelimab
- DRUG AB598
Study Locations (15)
Other
- Adelaide Cancer Research — Adelaide
- Queen Elizabeth Hospital — Adelaide
- National Cheng Kung University Hospital — Tainan
- Taipei Veterans General Hospital — Taipei
Florida
- Mayo Clinic Florida — Jacksonville
- Lake City Cancer Care, LLC. — Lake City
Ohio
- Gabrail Cancer Center (GCC) Canton Facility — Canton
- University Hospitals Cleveland Medical Center — Cleveland
Arizona
- Mayo Clinic Arizona — Phoenix
Illinois
- Affinity Health Hope and Healing Cancer Services, LLC — Hinsdale
Michigan
- Karmanos Cancer Institute — Detroit
Minnesota
- Mayo Clinic Rochester — Rochester
New Jersey
- Rutgers Cancer Institute of New Jersey — New Brunswick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2023-10-13 |
| Est. Completion | 2026-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05891171
The ClinicalTrials.gov registry entry for NCT05891171 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arcus Biosciences, which has 14 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 5 interventions — of which Fluorouracil is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05891171 reports 15 study locations spanning 10 distinct geographic areas — top geographies include Other, Florida, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05891171 about?
NCT05891171 is a clinical study titled "Study of AB598 Monotherapy and Combination Therapy in Participants With Advanced Cancers". The primary purpose of this study is to assess the safety and tolerability of AB598 in participants with advanced malignancies.
What is the current status of trial NCT05891171?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2023-10-13. Estimated completion is 2026-03.
What conditions does trial NCT05891171 study?
This clinical trial studies the following conditions: Ovarian Cancer, Bladder Cancer, Gastric Cancer, Cervical Cancer, Esophageal Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05891171?
The interventions under investigation include: Fluorouracil (DRUG), Leucovorin (DRUG), Oxaliplatin (DRUG), Zimberelimab (DRUG), AB598 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05891171?
This trial is sponsored by Arcus Biosciences, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05891171 being conducted?
This trial has 15 study locations across Arizona, Florida, Illinois, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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