Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingPhase 2interventionalRules rewrite

Phase 2: testing Nivolumab for Hepatocellular Carcinoma

This is a phase 2 single-arm, open-label clinical trial determining how well it works of cabozantinib in combination with ipilimumab/nivolumab and transarterial chemoembolization (TACE) in subjects with hepatocellular carcinoma (HCC). These are subjects who are not candidates for curative intent treatment.

Official registry: https://clinicaltrials.gov/study/NCT04472767 · University of California, Irvine · enrollment listed as 35

What this phase means

Phase 2: researchers already know a roughly safe dose (from phase 1). This stage asks whether the treatment actually helps the condition, and watches side effects more closely.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Nivolumab, Ipilimumab, or Cabozantinib. The registry lists allocation as na. This is a phase 2 single-arm, open-label clinical trial determining how well it works of cabozantinib in combination with ipilimumab/nivolumab and transarterial chemoembolization (TACE) in subjects with hepatocellular carcinoma (HCC).

They plan to enroll about 35 people at Orange. Taking part typically means taking a study drug (or dummy pill), a procedure as part of the study plus check-ins.

Official title (unrewritten)

Phase 2 Study of Cabozantinib Combined With Ipilimumab/Nivolumab and Transarterial Chemoembolization (TACE) in Patients With Hepatocellular Carcinoma (HCC) Who Are Not Candidates for Curative Intent Treatment

Interventions: Nivolumab, Ipilimumab, Cabozantinib, Transarterial Chemoembolization

Primary outcome (registry wording): Percentage of Participants with Progression-free Survival at 6 Months

Who it is for (from inclusion criteria)

  • Ages 18 Years to any
  • Histologic or radiographic diagnosis of hepatocellular carcinoma
  • At least one lesion amenable to TACE treatment
  • Child-Pugh A-B7 (B7 based on Albumin allowed)
  • Not a candidate for resection or transplantation
  • Performance status: how well you can do daily activities (ECOG score) ≤2
  • Must have at least one measurable lesion (either untreated or progressed after previous locoregional treatment)
  • Adequate organ and marrow function as defined below:

Public study contact (from the registry)

Chao Family Comprehensive Cancer Center University of California, Irvine

1-877-827-7883

ucstudy@uci.edu

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

Related recruiting trials in this snapshot

FAQ about this NCT record

Is NCT04472767 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT04472767?

Phase 2. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT04472767?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

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