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NCT06140134 · Rutgers, The State University of New Jersey

Liver Transplantation in Intrahepatic Cholangiocarcinoma

What this study is about

The aim of the current study is to determine the potential effectiveness of liver transplantation in the form of patients' how long patients live (OS) after neoadjuvant systemic therapy in patients with biologically responsive locally advanced non-metastatic intrahepatic cholangiocarcinoma (iCCA) in comparison to patients historically treated with chemotherapy alone.

View original scientific description

The aim of the current study is to determine the potential efficacy of liver transplantation in the form of patients' overall survival (OS) after neoadjuvant systemic therapy in patients with biologically responsive locally advanced non-metastatic intrahepatic cholangiocarcinoma (iCCA) in comparison to patients historically treated with chemotherapy alone.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Age ≥18 years of age on the day of consenting to the study.
  • Patients must have histologically confirmed diagnosis of locally advanced intrahepatic cholangiocarcinoma
  • Confirmed diagnosis of locally advanced unresectable iCCA with no vascular invasion, lymph node, or extrahepatic disease.
  • Unresectable disease based on tumor location or underlying liver disease
  • Patients must have ≥ 6 months of disease stability or tumor regression on neoadjuvant therapy. In cases in which patients had received second-line therapy, disease must also have been controlled for ≥ 6 months on that regimen.
  • Patients who had previous surgical resection for iCCA are eligible if surgery occurred more than 6 months prior to listing, and patients have had ≥ 6 months of disease stability or response on therapy.
  • ECOG performance status ≤1 (Karnofsky ≥70%, see Appendix A).
  • Patients must have organ and marrow function acceptable for liver transplantation per institutional protocol:
  • If history of chronic hepatitis B virus (HBV) infection, viral load should be undetectable on suppressive therapy.
  • If history of chronic hepatitis C virus (HCV) infection, patients should have undetectable HCV viral load.
  • Women of child-bearing years must have contraception plan in place from the time of study enrollment until at least one year following liver transplant.
  • Ability to understand and the willingness to sign a written informed consent document
  • Meets all other medical and psychosocial criteria for liver transplant
  • Demonstrate ability to comply with study procedures

Exclusion criteria

  • Age \<18 years of age on the day of consenting to the study.
  • Patients who have extrahepatic metastases, lymph node involvement, invasion or encasement of major hepatic vascular structures, perforation of the visceral peritoneum, invasion of extrahepatic structures, invasion of perihilar fat, periductular invasion, concurrent hepatoma or mixed hepatocellular cholangiocarcinoma.
  • Concurrent severe and/or uncontrolled concurrent illness including, but not limited to, ongoing or active infection, acute fulminant liver failure, symptomatic congestive heart failure, unstable angina pectoris, severe uncorrected coronary artery disease, severe cerebrovascular disease, severe pulmonary disease, or psychiatric illness/social situations that would limit compliance with study requirements and that would exclude the patient from eligibility for liver transplantation per institutional protocol.
  • Prior solid organ or bone marrow transplant
  • Dependent on ≥2 IV inotropic support to maintain hemodynamics
  • Previous (within the past 5 years) or concurrent presence of other cancer, except non-melanoma skin cancer and in situ carcinomas.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status Scale score \>1 (Karnofsky \<70%, see Appendix A).
  • Unable to understand and sign a written informed consent document
  • Untreated viral hepatitis
  • Pregnant or breast-feeding women
  • HIV-infected patients

Where

  • Newark, New Jersey

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Mar 20, 2026 · Source of record for eligibility and locations

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1 of 30 participants interested
3% interest

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A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

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Study locations

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RECRUITING

Newark

New Jersey

Location available
RECRUITING

Newark

New Jersey

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

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What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Intrahepatic Cholangiocarcinoma Treatment in Newark?

Join others in New Jersey exploring innovative treatment options through clinical research

Intrahepatic Cholangiocarcinoma Treatment Options in Newark, New Jersey

If you're searching for Intrahepatic Cholangiocarcinoma treatment in Newark, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Newark and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Intrahepatic Cholangiocarcinoma. All study-related care is provided at no cost to participants.

Local Sites
1 locations in New Jersey
Now Enrolling
Up to 30 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Intrahepatic Cholangiocarcinoma?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Intrahepatic Cholangiocarcinoma

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Intrahepatic Cholangiocarcinoma Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT06140134. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.