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RECRUITING Phase 2

Study of Safety/Feasibility of a Hybrid Model of Tertiary and Community Delivery of Hepatic Artery Infusion Chemotherapy

NCT07201519 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to help learn about the safety and feasibility of hepatic artery infusion chemotherapy for those who have colorectal liver metastases, both resectable and unresectable, or unresectable intrahepatic cholangiocarcinoma. The main questions it aims to answer are: * safety and feasibility of installing a pump that deliveries chemotherapy to the hepatic artery (the blood vessel that supplies blood to the liver) * help learn more about the safety of patients having pump refills at home or a local clinic versus having it routinely done at the hospital Participants will have surgery to install a pump which is a standard surgical procedure. After surgery, participants will select to either receive treatment at the hospital facility or with a community oncologist that will provide cancer care to participants close to home, rather than in a large hospital or academic medical center. The main treatment on study will last about 3-4 months.

Interventions

  • DEVICE Hepatic Artery Infusion Pump (HAIP)
  • PROCEDURE Standard Treatment
  • PROCEDURE Community Treatment
  • DRUG Systemic Chemotherapy Standard of Care
  • DRUG Standard Of Care targeting driver mutations

Study Locations (1)

Kentucky

  • University of Kentucky — Lexington

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2026-01-23
Est. Completion 2030-02
Phase Phase 2

Sponsor

Michael J Cavnar, MD

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07201519

The ClinicalTrials.gov registry entry for NCT07201519 describes a study currently listed as 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 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Michael J Cavnar, MD, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Colorectal Cancer Metastatic appearing as the primary indexed condition, and to 5 interventions — of which Hepatic Artery Infusion Pump (HAIP) 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: NCT07201519 reports 1 study location spanning 1 distinct geographic area — top geographies include Kentucky. 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 NCT07201519 about?

NCT07201519 is a clinical study titled "Study of Safety/Feasibility of a Hybrid Model of Tertiary and Community Delivery of Hepatic Artery Infusion Chemotherapy". The goal of this clinical trial is to help learn about the safety and feasibility of hepatic artery infusion chemotherapy for those who have colorectal liver metastases, both resectable and unresectable, or unresectable intrahepatic cholangiocarcinoma. The main questions it aims to answer are: * sa...

What is the current status of trial NCT07201519?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 80 participants. The study started on 2026-01-23. Estimated completion is 2030-02.

What conditions does trial NCT07201519 study?

This clinical trial studies the following conditions: Colorectal Cancer Metastatic, Intrahepatic Cholangiocarcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07201519?

The interventions under investigation include: Hepatic Artery Infusion Pump (HAIP) (DEVICE), Standard Treatment (PROCEDURE), Community Treatment (PROCEDURE), Systemic Chemotherapy Standard of Care (DRUG), Standard Of Care targeting driver mutations (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07201519?

This trial is sponsored by Michael J Cavnar, MD, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07201519 being conducted?

This trial has 1 study location across Kentucky. 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