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Completed Phase 3 Interventional

Percutaneous Hepatic Perfusion in Patients With Hepatic-dominant Ocular Melanoma

ClinicalTrials.gov ID: NCT02678572

Public ClinicalTrials.gov record NCT02678572. 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 2, 2026, 4:38 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

A Single-arm, Multi-Center, Open-Label Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Melphalan/HDS Treatment in Patients With Hepatic-Dominant Ocular Melanoma

Brief summary

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

This study will evaluate patients who have melanoma that has spread from the eye to the liver: Patients in the study will be treated with Melphalan/HDS up to 6 total treatment, and will be followed until death. This study will evaluate the safety and effects of the treatment on how long patients live and how long it takes for the cancer to advance or respond to the treatment.

Study identification

NCT ID
NCT02678572
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Delcath Systems Inc.
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Combination Product

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
Jan 31, 2016
Primary completion
May 17, 2023
Completion
Aug 14, 2023
Last update posted
Dec 20, 2023

2016 – 2023

United States locations

U.S. sites
10
U.S. states
10
U.S. cities
10
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85719
Stanford University Palo Alto California 19380
Moffitt Cancer Center Tampa Florida 33612
Emory University Atlanta Georgia 30322
University of Chicago Chicago Illinois 60637
Roswell Park Cancer Institute Buffalo New York 14263
Duke University Medical Center Durham North Carolina 27710
Ohio State University James Cancer Center Columbus Ohio 43210
Thomas Jefferson University Philadelphia Pennsylvania 19107
University of Tennessee Health Science Center Memphis Tennessee 38163

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02678572, 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 Dec 20, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02678572 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →