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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

Short Title: C6461013


Enrollment Status: Recruiting

NCT #: NCT07227012

Specialty Area: Oncology

Condition Studied: Unresectable Locally Advanced or Metastatic Hepatocellular Carcinoma (HCC)

Age Groups: Adult; Older Adult

Phase: I/II


Study Information

Summary / Purpose

This research study is evaluating a new investigational treatment for patients with advanced Hepatocellular carcinoma, the most common type of liver cancer. The study will look at the safety and effectiveness of the investigational drug PF-08634404 when given alone or in combination with the immunotherapy medicine Ipilimumab. Researchers want to learn whether these treatments can help slow or stop the growth of liver cancer and better understand possible side effects. Information from this study may help improve future treatment options for patients with advanced liver cancer.

Study Type: Interventional
Accepts Healthy Volunteers: No

Who Can Participate

Eligibility Criteria:
  • Adults 18+ years of age
  • Diagnosed with unresectable or metastatic Hepatocellular carcinoma
  • Have at least one measurable tumor on imaging
  • No significant uncontrolled medical conditions
  • No active serious infections
  • No history of severe autoimmune disease requiring immunosuppression
  • No prior organ transplantation or other conditions that would make participation unsafe or interfere with study results

What's Involved

Participation in the study will include:
  • Receiving the study treatment, which may include the investigational drug PF-08634404 alone or in combination with Ipilimumab, given through intravenous (IV) infusion
  • Attending regular visits for monitoring, including physical exams, blood tests, and scans to see how the cancer is responding and to check for side effects.
  • Attending follow-up visits after treatment ends.

Principal Investigator

Additional Information

Location: Renown Health, Office of Clinical Research
Address:

1500 E 2nd St. Reno, NV 89502

General Research: 775-982-3646
Oncology Research: 775-982-5050
Email: Renown-CRD@renown.org

Disclaimer: This listing gives you general information about the study and isn't part of the official consent process. If you decide to learn more, the research team will talk with you and check if you meet any additional requirements to join the study.

ER Wait Times

How are wait times calculated?

Our estimated ER wait times reflect the average time from check-in to being seen by a medical professional during triage, where patients are prioritized based on the severity of their condition.

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