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Terminated Phase 4 Interventional

HD IL-2 + Vemurafenib in Patients With BRAF Mutation Positive Metastatic Melanoma

ClinicalTrials.gov ID: NCT01683188

Public ClinicalTrials.gov record NCT01683188. 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 May 11, 2026, 9:28 PM 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 Multi-Center Study of High Dose Aldesleukin (Interleukin-2) + Vemurafenib Therapy in Patients With BRAFV600 Mutation Positive Metastatic Melanoma

Study identification

NCT ID
NCT01683188
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Clinigen, Inc.
Industry
Enrollment
53 participants

Conditions and interventions

Interventions

  • vemurafenib + HD IL-2 Drug

Drug

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
Jul 31, 2012
Primary completion
Oct 31, 2014
Completion
Oct 31, 2014
Last update posted
Jan 31, 2021

2012 – 2014

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
University Arizona Cancer Center Tucson Arizona 85719
Moores UCSD Cancer Center La Jolla California 92093
MSMC Research Program Miami Beach Florida 33140
Emory University School of Medicine Atlanta Georgia 30322
Loyola University Medical Center, Div of Hematology/Oncology Maywood Illinois 60153
Luther General Cancer Care Institute Park Ridge Illinois 60068
Indiana University Indianapolis Indiana 46202
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
University of Kansas Kansas City Kansas 66160-0003
Hematology/Oncology Clinic Baton Rouge Louisiana 70809
University of Michigan, Comprehensive Cancer Center Ann Arbor Michigan 48109
Karmanos Cancer Institute Detroit Michigan 48201
University of Minnesota Masonic Cancer Center Minneapolis Minnesota 55455
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601
Columbia University Medical Center, Herbert Irving Comprehensive Cancer Center New York New York 10032
The Christ Hospital Cancer Center Cincinnati Ohio 45219
Case Comprehensive Cancer Center Cleveland Ohio 44106
Providence Cancer Center Portland Oregon 97213
St. Luke's Hospital, Anderson Campus Easton Pennsylvania 18045
UPMC Cancer Centers Pittsburgh Pennsylvania 15232

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01683188, 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 Jan 31, 2021 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01683188 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →