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Recruiting Phase 1Phase 2 Interventional

Symbiotic-GI-13: A Study to Learn About Study Medicine Called PF-08634404 as a Single Treatment and Combination Treatment in Adult Participants With a Liver Cancer Called Hepatocellular Carcinoma, That is Too Advanced to be Removed by Surgery and May Have Spread to Other Parts of the Body.

ClinicalTrials.gov ID: NCT07227012

Public ClinicalTrials.gov record NCT07227012. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 5:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

AN INTERVENTIONAL OPEN-LABEL PHASE 1B/2 STUDY TO EVALUATE SAFETY, PHARMACOKINETICS, AND PRELIMINARY EFFICACY OF PF-08634404 AS MONOTHERAPY AND COMBINATION THERAPY IN ADULT PARTICIPANTS WITH UNRESECTABLE LOCALLY ADVANCED OR METASTATIC HEPATOCELLULAR CARCINOMA

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to learn about the effects of study medicine (PF-08634404) when given alone or with another antibody (ipilimumab) for the treatment of a type of liver cancer called hepatocellular carcinoma (HCC) that is either locally advanced (spread to nearby tissues) or has spread to other parts of the body. To join the study, participants must meet the following conditions: * Be 18 years or older. * Have locally advanced or metastatic HCC. * Is not a candidate for complete surgical or loco-regional therapies. * Have not received any whole-body treatment for HCC. Participants will receive PF-08634404 either alone or in combination with ipilimumab. The medicine will be given through intravenous (IV) infusions, which means it will be administered directly into a vein. All treatments will take place at clinical trial sites, where trained medical staff will monitor participants during and after each visit.

Study identification

NCT ID
NCT07227012
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
138 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2025
Primary completion
Oct 17, 2027
Completion
Oct 16, 2028
Last update posted
Aug 16, 2026

2025 – 2028

United States locations

U.S. sites
41
U.S. states
8
U.S. cities
22
Facility City State ZIP Site status
Chao Family Comprehensive Cancer Center and Ambulatory Care Irvine California 92612 Recruiting
UCI Health - Irvine Infusion Pharmacy ACC Irvine California 92612 Recruiting
UCI Health - Irvine Irvine California 92612 Recruiting
Keck Hospital of USC Los Angeles California 90033 Recruiting
Los Angeles General Medical Center Los Angeles California 90033 Recruiting
USC/Norris Comprehensive Cancer Center / Investigational Drug Services Los Angeles California 90033 Recruiting
USC/Norris Comprehensive Cancer Center Los Angeles California 90033 Recruiting
UC Irvine Health - Chao Family Comprehensive Cancer Center Orange California 92868 Recruiting
Keck Medical Center of USC Pasadena Pasadena California 91105 Recruiting
Moffitt Cancer Center at Speros Land O' Lakes Florida 34638 Recruiting
Moffitt Cancer Center at SouthShore Ruskin Florida 33570 Recruiting
Moffitt Cancer Center - International Plaza Tampa Florida 33607 Recruiting
Moffitt Cancer Center - McKinley Campus Tampa Florida 33612 Recruiting
Moffitt Cancer Center Tampa Florida 33612 Recruiting
Moffitt McKinley Hospital Tampa Florida 33612 Recruiting
Moffitt Cancer Center at Wesley Chapel Wesley Chapel Florida 33544 Recruiting
Memorial Hospital Shiloh Illinois 62269 Recruiting
Siteman Cancer Center - Shiloh Shiloh Illinois 62269 Recruiting
Allina Health Cancer Institute - Mercy Hospital Coon Rapids Minnesota 55433 Recruiting
Allina Health Cancer Institute - Abbott Northwestern Hospital Minneapolis Minnesota 55407 Recruiting
Allina Health Cancer Institute - United Hospital Saint Paul Minnesota 55102 Recruiting
Siteman Cancer Center - St. Peters City of Saint Peters Missouri 63376 Recruiting
Siteman Cancer Center - West County Creve Coeur Missouri 63141 Recruiting
Siteman Cancer Center - North County Florissant Missouri 63031 Recruiting
Saint Luke's Cancer Institute Kansas City Missouri 64111 Recruiting
Saint Luke's Hospital of Kansas City Kansas City Missouri 64111 Recruiting
Siteman Cancer Center St Louis Missouri 63108 Recruiting
Barnes-Jewish Hospital St Louis Missouri 63110 Recruiting
Washington University School of Medicine - Siteman Cancer Center St Louis Missouri 63110 Recruiting
Siteman Cancer Center - South County St Louis Missouri 63129 Recruiting
Renown Health Medical Oncology Reno Nevada 89502 Recruiting
Renown Office of Clinical Research Reno Nevada 89502 Recruiting
Renown Regional Medical Center Reno Nevada 89502 Recruiting
Duke Cancer Center Cary Cary North Carolina 27518 Recruiting
Duke Cancer Center - Investigational Chemotherapy Service Durham North Carolina 27710 Recruiting
Duke Cancer Center Durham North Carolina 27710 Recruiting
Duke University - Main Hospital and Clinics Durham North Carolina 27710 Recruiting
Duke Cancer Center Raleigh Raleigh North Carolina 27609 Recruiting
Virginia Mason Medical Center Seattle Washington 98101 Not yet recruiting
Fred Hutchinson Cancer Center Seattle Washington 98109 Recruiting
University of Washington Medical Center- Montlake Seattle Washington 98195 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07227012, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 16, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07227012 live on ClinicalTrials.gov.

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