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CompletedNCT00003647Updated Jul 25, 2008

Chemotherapy With or Without Immunotherapy in Treating Patients With Stage III or Stage IV Melanoma

A Phase 3 interventional study of allovectin-7 and allovectin-7/dacarbazine in Stage IV Melanoma, Stage III Melanoma and Recurrent Melanoma, sponsored by Vical. Completed at 44 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-07-25.

Sponsored by Vical · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Ages
18 Years and older
01

Study summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Injecting allovectin-7 into a person's melanoma cells may make the body build an immune response that will kill tumor cells.

PURPOSE: Randomized phase III trial to compare the effectiveness of dacarbazine with or without immunotherapy in treating patients who have stage III or stage IV melanoma.

Read the detailed description

OBJECTIVES: I. Demonstrate either an improvement in the median time to disease progression by at least 2 months with no decrease in the rate of objective clinical response OR an improvement by at least 15% in the rate of objective clinical response with no decrease in the median time to disease progression in patients with stage III or IV melanoma receiving dacarbazine with Allovectin-7 when compared with patients receiving dacarbazine alone.

II. Determine the benefits, risks, and side effects of these regimens in this patient population.

PROTOCOL OUTLINE: This is a randomized, multicenter study. Patients are stratified according to sex, age, and spread of disease (cutaneous or nodal vs visceral disease). Patients are randomized to one of two treatment arms.

Arm I: Patients receive dacarbazine IV over 1 hour on day 0. Arm II: Patients receive treatment as in arm I. Patients also receive Allovectin-7 intratumorally on days 3 and 10.

Patients with stable or responding disease may receive additional courses every 28 days.

Patients are followed every 4 months.

PROJECTED ACCRUAL:

A total of 280 patients (140 in each arm) will be accrued for this study.

02

Conditions studied

  • Stage IV Melanoma
  • Stage III Melanoma
  • Recurrent Melanoma

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Keywords

  • adult solid tumor
  • body system/site cancer
  • cancer
  • melanoma
  • recurrent melanoma
  • skin tumor
  • solid tumor
  • stage III melanoma
  • stage IV melanoma
  • stage, melanoma
03

In context

Melanoma

3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.

Browse Melanoma studies →

Lead sponsor

Vical is the lead sponsor of 13 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older

Eligibility criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

  • Histologically confirmed stage III or IV melanoma 1 or more metastatic tumors for which surgery is not deemed to be a curative option
  • Dacarbazine is indicated as first line chemotherapy
  • At least 1 measurable tumor at least 1 cm2 but no greater than 100 cm2
  • No history of brain metastases

--Prior/Concurrent Therapy--

  • Biologic therapy: At least 4 weeks since prior biologic therapy
  • Chemotherapy: See Disease Characteristics; No prior chemotherapy
  • Endocrine therapy: No concurrent immunosuppressive drugs
  • Radiotherapy: At least 4 weeks since prior radiotherapy
  • Surgery: At least 2 weeks since prior major surgery
  • Other: No other concurrent anticancer drug therapy or experimental therapy

--Patient Characteristics--

  • Age: 18 and over
  • Performance status: Karnofsky 80-100%
  • Life expectancy: At least 24 weeks
  • Hematopoietic: WBC at least 3,000/mm3; Platelet count at least 100,000/mm3; Hemoglobin at least 9 g/dL
  • Hepatic: Bilirubin no greater than 2.0 mg/dL; SGOT/SGPT less than 3 times upper limit of normal (ULN); PT/PTT normal; Albumin normal; LDH no greater than 2 times ULN
  • Renal: Creatinine no greater than 2.0 mg/dL
  • Cardiovascular: No uncontrolled hypertension; No New York Heart Association class III or IV disease
  • Other: HIV negative; Not pregnant or nursing; Negative pregnancy test; Fertile patients must use effective contraception; No active autoimmune disease; No active infection requiring parenteral antibiotics; No uncontrolled diabetes mellitus; No other prior malignancy within the past 5 years except skin cancer or stage 0-II cervical cancer; No significant psychiatric disorders
05

Study design

Phase
Phase 3
Primary purpose
Treatment

Interventions

  • Drugallovectin-7
  • Drugallovectin-7/dacarbazine
  • Drugdacarbazine
06

Study locations

44 sites
  • University of Arkansas for Medical Sciences
    Little Rock, Arkansas 72205, United States
  • Comprehensive Blood and Cancer Center
    Bakersfield, California 93309, United States
  • Scripps Memorial Hospitals-Stevens Cancer Center - Encinitas
    Encinitas, California 92023, United States
  • Kaiser Permanente-Southern California Permanente Medical Group
    San Diego, California 92120, United States
  • Yale Comprehensive Cancer Center
    New Haven, Connecticut 06520-8028, United States
  • Washington Cancer Institute
    Washington, District of Columbia 20010, United States
  • Mount Sinai Comprehensive Cancer Center
    Miami Beach, Florida 33140, United States
  • H. Lee Moffitt Cancer Center and Research Institute
    Tampa, Florida 33612-9497, United States
  • Georgia Cancer Specialists
    Decatur, Georgia 30033, United States
  • Georgia Cancer Specialists, P.C.
    East Point, Georgia 30344, United States
  • St. Francis Medical Center
    Honolulu, Hawaii 96817, United States
  • Robert H. Lurie Comprehensive Cancer Center, Northwestern University
    Chicago, Illinois 60611-3013, United States
  • Lutheran General Hospital
    Park Ridge, Illinois 60068, United States
  • Cancer Care Center for Southern Indiana
    Bloomington, Indiana 47403, United States
  • Cancer Care Center
    New Albany, Indiana 47150, United States
  • Oncology and Hematology Associates
    Westwood, Kansas 66205, United States
  • Lucille Parker Markey Cancer Center, University of Kentucky
    Lexington, Kentucky 40536-0093, United States
  • Louisiana State University School of Medicine
    New Orleans, Louisiana 70112-2822, United States
  • Franklin Square Hospital Center
    Baltimore, Maryland 21237, United States
  • Providence Hospital Cancer Center
    Southfield, Michigan 48075, United States
  • Virginia Piper Cancer Institute
    Minneapolis, Minnesota 55407, United States
  • North Memorial Health Care
    Robbinsdale, Minnesota 55422, United States
  • Mayo Clinic Cancer Center
    Rochester, Minnesota 55905, United States
  • Park Nicollet Clinic
    St. Louis Park, Minnesota 55416, United States
  • St. Louis University Health Sciences Center
    Saint Louis, Missouri 63110-0250, United States
  • Missouri Baptist Cancer Center
    Saint Louis, Missouri 63131, United States
  • Billings Interhospital Oncology Project
    Billings, Montana 59101, United States
  • Bergan Mercy Medical Center
    Omaha, Nebraska 68124, United States
  • Norris Cotton Cancer Center
    Lebanon, New Hampshire 03756-0002, United States
  • HemOnCare, P.C.
    Brooklyn, New York 11235, United States
  • Arena Oncology Associates
    Great Neck, New York 11021, United States
  • Beth Israel Medical Center
    New York, New York 10003, United States
  • Mount Sinai School of Medicine
    New York, New York 10029, United States
  • Comprehensive Cancer Center at Wake Forest University
    Winston-Salem, North Carolina 27157-1082, United States
  • Mid Dakota Clinic, P.C.
    Bismarck, North Dakota 58501, United States
  • Mid-Ohio Oncology/Hematology, Inc.
    Columbus, Ohio 43222, United States
  • Toledo Clinic, Inc.
    Toledo, Ohio 43623, United States
  • University of Pennsylvania Cancer Center
    Philadelphia, Pennsylvania 19104-4283, United States
  • Cancer Centers of the Carolinas
    Greenville, South Carolina 29605, United States
  • Huntsman Cancer Institute
    Salt Lake City, Utah 84112, United States
  • Danville Hematology and Oncology, Inc.
    Danville, Virginia 24541, United States
  • Cancer Treatment Centers of America in Hampton Roads
    Portsmouth, Virginia 23704, United States
  • Seattle Cancer Care Alliance
    Seattle, Washington 98109, United States
  • Medical College of Wisconsin
    Milwaukee, Wisconsin 53226, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00003647
Lead sponsor
Vical
First posted
Mar 23, 2004
Start date
Jul 1998
Completion
Sep 2002
Last update
Jul 25, 2008

Study contacts

Cherie Smith
study chair · Vical

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2008. You cannot join it, but the record below documents what was studied.

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