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A Phase III Randomized Double-Blind Pivotal Trial of Immunotherapy With a Polyvalent Melanoma Vaccine, CancerVax™ Vaccine Plus BCG Versus Placebo Plus BCG as a Post-Surgical Treatment for Stage IV Melanoma
This is a Phase III study in patients with melanoma that has spread to the lymph nodes and/or a distant organ, and who have had all of their cancer surgically removed. The purpose of this study is to evaluate the ability of the CancerVax™ vaccine to prevent or slow the recurrence of melanoma.
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
Arizona Cancer Center
Tucson, Arizona, United States
Central Arkansas Veterans Healthcare System
Little Rock, Arkansas, United States
University of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
Kaiser Permanente Medical Group
Anaheim, California, United States
Cedars Sinai Comprehensive Cancer Center
Los Angeles, California, United States
Hoag Memorial Hospital Presbyterian
Newport Beach, California, United States
Comprehensive Cancer Center at DRMC
Palm Springs, California, United States
Kaiser Permanente Medical Group
Riverside, California, United States
Kaiser Permanente Medical Group
San Diego, California, United States
Sharp Hospital
San Diego, California, United States
Last Updated
June 24, 2005
670
Estimated participants
CancerVax vaccine (CANVAXIN)
BIOLOGICAL
Lead Sponsor
CancerVax Corporation
NCT07371663
NCT01898039
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06209580