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ACTIVE NOT RECRUITING Phase 2

A Study to Determine Whether Chemotherapy and Atezolizumab is Better Than Chemotherapy, Bevacizumab and Atezolizumab in Patients With Advanced Liver Cancer

NCT05211323 · View on ClinicalTrials.gov ↗

Study Summary

This phase II trial compares the effect of adding bevacizumab and atezolizumab to gemcitabine and cisplatin (chemotherapy) versus chemotherapy and atezolizumab in treating patients with liver cancer that cannot be removed by surgery (unresectable) or that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the formation of blood vessels that bring oxygen and nutrients to tumor. This may slow the growth and spread of tumor. Chemotherapy drugs, such as gemcitabine and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving bevacizumab and atezolizumab with chemotherapy may kill more tumor cells in patients liver cancer than chemotherapy and atezolizumab.

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Computed Tomography
  • BIOLOGICAL Atezolizumab
  • DRUG Cisplatin
  • BIOLOGICAL Bevacizumab

Study Locations (20)

California

  • Sutter Auburn Faith Hospital — Auburn
  • Alta Bates Summit Medical Center-Herrick Campus — Berkeley
  • Palo Alto Medical Foundation-Fremont — Fremont
  • Memorial Medical Center — Modesto
  • Palo Alto Medical Foundation-Camino Division — Mountain View
  • Palo Alto Medical Foundation Health Care — Palo Alto
  • Sutter Roseville Medical Center — Roseville
  • Sutter Medical Center Sacramento — Sacramento
  • California Pacific Medical Center-Pacific Campus — San Francisco
  • Palo Alto Medical Foundation-Santa Cruz — Santa Cruz
  • Palo Alto Medical Foundation-Sunnyvale — Sunnyvale
  • Sutter Solano Medical Center/Cancer Center — Vallejo

Illinois

  • Carle at The Riverfront — Danville
  • Carle Physician Group-Effingham — Effingham
  • Carle Physician Group-Mattoon/Charleston — Mattoon
  • Carle Cancer Center — Urbana
  • The Carle Foundation Hospital — Urbana

Iowa

  • UI Health Care Mission Cancer and Blood - Ankeny Clinic — Ankeny
  • Iowa Methodist Medical Center — Des Moines

Indiana

  • Memorial Hospital of South Bend — South Bend

Trial Details

FieldValue
Enrollment Target 88 participants
Start Date 2022-12-07
Est. Completion 2026-06-30
Phase Phase 2

Sponsor

National Cancer Institute (NCI)

2,390 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05211323

The ClinicalTrials.gov registry entry for NCT05211323 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 88 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Cancer Institute (NCI), which has 2,390 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Stage IV Liver Cancer appearing as the primary indexed condition, and to 5 interventions — of which Biospecimen Collection 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: NCT05211323 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Illinois, Iowa. 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 NCT05211323 about?

NCT05211323 is a clinical study titled "A Study to Determine Whether Chemotherapy and Atezolizumab is Better Than Chemotherapy, Bevacizumab and Atezolizumab in Patients With Advanced Liver Cancer". This phase II trial compares the effect of adding bevacizumab and atezolizumab to gemcitabine and cisplatin (chemotherapy) versus chemotherapy and atezolizumab in treating patients with liver cancer that cannot be removed by surgery (unresectable) or that may have spread from where it first started ...

What is the current status of trial NCT05211323?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 88 participants. The study started on 2022-12-07. Estimated completion is 2026-06-30.

What conditions does trial NCT05211323 study?

This clinical trial studies the following conditions: Stage IV Liver Cancer, Combined Hepatocellular Carcinoma and Cholangiocarcinoma, Stage III Liver 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 NCT05211323?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Computed Tomography (PROCEDURE), Atezolizumab (BIOLOGICAL), Cisplatin (DRUG), Bevacizumab (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05211323?

This trial is sponsored by National Cancer Institute (NCI), which has 2,390 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05211323 being conducted?

This trial has 20 study locations across California, Illinois, Indiana, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial