NCT00518895

Brief Summary

This study is being performed to prospectively determine whether dacarbazine plus Genasense is significantly better than dacarbazine plus placebo in chemotherapy-naive patients with advanced melanoma and low baseline LDH (LDH less than or equal to 0.8 times the upper limit of normal). LDH is a biomarker strongly associated with improved outcomes in a recent trial of dacarbazine plus Genasense.

Trial Health

98
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P50-P75 for phase_3

Timeline
Completed

Started Jul 2007

Typical duration for phase_3

Geographic Reach
11 countries

74 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2007

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

August 14, 2007

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 21, 2007

Completed
3.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2011

Completed
Last Updated

November 7, 2011

Status Verified

April 1, 2009

Enrollment Period

3.8 years

First QC Date

August 14, 2007

Last Update Submit

November 4, 2011

Conditions

Keywords

MelanomaAdvanced MelanomaMalignant MelanomaMetastatic MelanomaSkin CancerGenasenseoblimersenantisenseBcl-2 antisenseG3139dacarbazine

Outcome Measures

Primary Outcomes (1)

  • Progression-free survival and overall survival

    Every 42 days from date of randomization during protocol therapy

Secondary Outcomes (1)

  • Response rate, durable response rate, duration of response, safety

    Response and progression every 42 days from date of randomization during protocol therapy

Study Arms (2)

A

EXPERIMENTAL

Dacarbazine with Genasense

Drug: dacarbazine plus Genasense

B

ACTIVE COMPARATOR

Dacarbazine with placebo

Drug: dacarbazine plus placebo

Interventions

Protocol therapy will be administered in 21-day cycles for up to 8 cycles. Subjects in the dacarbazine plus Genasense group will receive Genasense 7 mg/kg/day by continuous intravenous infusion beginning on Day 1 and continuing for 5 days (120 hours) plus dacarbazine 1000 mg/m2 as a 60-minute intravenous infusion immediately following the conclusion of the Genasense infusion. Subjects who are responding or have stable disease after 8 cycles of therapy may, at the Investigator's discretion, continue that same therapy for up to 8 additional cycles.

Also known as: dacarbazine plus Genasense (oblimersen, G3139)
A

Protocol therapy will be administered in 21-day cycles for up to 8 cycles. Subjects in the dacarbazine plus placebo group will receive placebo (that is, locally available commercial 0.9% Sodium Chloride Injection) by continuous intravenous infusion beginning on Day 1 and continuing for 5 days (120 hours) plus dacarbazine 1000 mg/m2 as a 60-minute intravenous infusion immediately following the conclusion of the placebo infusion. Subjects who are responding or have stable disease after 8 cycles of therapy may, at the Investigator's discretion, continue that same therapy for up to 8 additional cycles.

Also known as: dacarbazine plus placebo (0.9% Sodium Chloride Injection)
B

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Histologically confirmed diagnosis of melanoma
  • Progressive disease that is not surgically resectable, or metastatic Stage IV
  • Low-normal LDH, defined as ≤ 0.8 times the upper limit of normal
  • No prior chemotherapy
  • Measurable disease
  • ECOG performance status ≤ 1
  • At least 4 weeks and recovery from effects of major prior surgery or other therapy, including immunotherapy, radiation therapy, or cytokine, biologic or vaccine therapy
  • Prior immunotherapy allowed
  • Adequate organ function

You may not qualify if:

  • Prior cytotoxic chemotherapy, including regional perfusion, or prior Genasense treatment
  • Primary ocular or mucosal melanoma
  • Bone-only metastatic disease
  • History or presence of brain metastasis or leptomeningeal disease
  • Significant medical disease other than cancer
  • Organ allograft

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (77)

University of South Alabama Hospital, Mitchell Cancer Institute

Mobile, Alabama, 36607, United States

Location

San Diego Pacific Oncology and Hematology Associates Inc.

Encinitas, California, 92024, United States

Location

Redwood Regional Medical Group, Inc.

Santa Rosa, California, 95403, United States

Location

Siouxland Hematology Oncology Associates

Sioux City, Iowa, 51101, United States

Location

Dana Farber Cancer Institute

Boston, Massachusetts, 02115, United States

Location

Hematology Oncology Centers of the Northern Rockies

Billings, Montana, 59101, United States

Location

Morristown Memorial - Atlantic Healthcare System

Morristown, New Jersey, 07960, United States

Location

Cancer Care Associates

Oklahoma City, Oklahoma, 73112, United States

Location

Cancer Care Associates, Site 1

Tulsa, Oklahoma, 74104, United States

Location

St. Luke's Cancer Center

Bethlehem, Pennsylvania, 18015, United States

Location

Thomas Jefferson University Hospital

Philadelphia, Pennsylvania, 19107, United States

Location

The West Clinic

Memphis, Tennessee, 38120, United States

Location

Texas Oncology - Sammons Cancer Center

Dallas, Texas, 75246, United States

Location

MD Anderson Cancer Center at University of Texas

Houston, Texas, 77030-4009, United States

Location

Sydney Cancer Center, Royal Prince Alfred Hospital

Camperdown, New South Wales, 2050, Australia

Location

Calvary Mater Newcastle

Newcastle, New South Wales, Australia

Location

Westmead Hospital

Westmead, New South Wales, Australia

Location

Universitatsklinik fur Dermatologie und Venerologie, Medizinische Universitat Innsbruck

Innsbruck, Austria

Location

Landesklinikum St. Polten

Sankt Pölten, Austria

Location

Medical University of Vienna, Vienna General Hospital

Vienna, Austria

Location

London Regional Cancer Program

London, Ontario, Canada

Location

Princess Margaret Hospital

Toronto, Ontario, Canada

Location

Charles University, Dermatology Department

Prague, Czechia

Location

CHU Saint Jacques

Besançon, France

Location

Hopital Saint-Andre

Bordeaux, France

Location

CHU Ambroise Pare

Boulogne-Billancourt, France

Location

CHU Hotel Dieu

Clermont-Ferrand, France

Location

CHU de Dijon, Hopital du Bocage Sud

Dijon, France

Location

CHU de Grenoble, Hopital Albert Michallon

Grenoble, France

Location

Centre Hospitalier du Mans

Le Mans, France

Location

CHRU de Lille, Hopital Claude Huriez

Lille, France

Location

Hopital de l'Hotel Dieu

Lyon, France

Location

Hopital Sainte Marguerite

Marseille, France

Location

Hopital Saint Eloi

Montpellier, France

Location

CHU Hotel Dieu

Nantes, France

Location

Hopital Saint-Louis

Paris, France

Location

Hopital Robert Debre

Reims, France

Location

CHU CH Nicolle

Rouen, France

Location

Institut Gustave Roussy

Villejuif, France

Location

Charite Universitatsmedizin Berlin

Berlin, Germany

Location

Vivantes Klinikum im Friedrichshain

Berlin, Germany

Location

Vivantes Klinikum Neukoln, Klinik fur Dermatologie und Venerologie

Berlin, Germany

Location

Klinik fur Dermatologie und Allergologie der Ruhr-Universitat Bochum

Bochum, Germany

Location

Klinik und Poliklinik fur Dermatologie und Venerologie

Cologne, Germany

Location

Helios Klinikum Erfurt

Erfurt, Germany

Location

Klinik fur Dermatologie, Allergologie und Venerologie, Universitatsklinikum Essen

Essen, Germany

Location

Universitatsklinikum Freiburg

Freiburg im Breisgau, Germany

Location

Hautklinik Linden

Hanover, Germany

Location

Klinikum der Friedrich-Schiller-Universitat Jena

Jena, Germany

Location

Universitatklinikum A. o. R.

Leipzig, Germany

Location

Hospital of the University of Schleswig-Holstein

Lübeck, Germany

Location

Universitats-Hautklinik Mainz

Mainz, Germany

Location

Universitatsklinikum Mannheim

Mannheim, Germany

Location

Universitatsklinikum Giessen und Marburg GmbH, Klinik fur Dermatologie und Allergologie

Marburg, Germany

Location

Klinik und Poliklinik fur Hautkrankheiten

Münster, Germany

Location

Helios Vogtland-Klinikum Plauen

Plauen, Germany

Location

Klinikum Quedlinburg

Quedlinburg, Germany

Location

Dermatologische Klinik und Poliklinik

Regensburg, Germany

Location

Hautklinik Universitat Tubingen

Tübingen, Germany

Location

Ospedale San Salvatore

Coppitto-L'Aquila, Italy

Location

Istituto Nazionale dei Tumori

Milan, Italy

Location

Istituto Nazionale dei Tumori "G. Pascale"

Napoli, Italy

Location

IFO Instituto Regina-Elena - IRCCS

Rome, Italy

Location

Istituto Dermopatico dell'Immacolata

Rome, Italy

Location

Azienda Ospedaliera Universitaria di Siena

Siena, Italy

Location

Szpital Akademii Medycznej w Gdansku

Gdansk, Poland

Location

Wielkopolskie Centrum Onkologii

Poznan, Poland

Location

Hospital Clinic I Provincial de Barcelona

Barcelona, Spain

Location

Hospital Germans Trias I Pujol

Barcelona, Spain

Location

Hospital Gregorio Maranon

Madrid, Spain

Location

Clinica Universitaria de Navarra

Navarra, Spain

Location

University Hospital Zurich

Zurich, Switzerland

Location

Guy's Hospital

London, United Kingdom

Location

The Royal Marsden Hospital

London, United Kingdom

Location

Christie Hospital

Manchester, United Kingdom

Location

Nottingham University Hospitals NHS Trust, City Campus

Nottingham, United Kingdom

Location

Weston Park Hospital

Sheffield, United Kingdom

Location

Related Publications (2)

  • Bedikian AY, Agarwala SS, Gilles E, Itri L, Kay R, Garbe C. The AGENDA Study: A randomized, double-blind study of Genasense plus dacarbazine (DTIC) in chemotherapy-naïve subjects with advanced melanoma and low LDH. Pigment Cell Res. 2007;20:538 [Abstract T-26].

    BACKGROUND
  • Bedikian AY, Millward M, Pehamberger H, Conry R, Gore M, Trefzer U, Pavlick AC, DeConti R, Hersh EM, Hersey P, Kirkwood JM, Haluska FG; Oblimersen Melanoma Study Group. Bcl-2 antisense (oblimersen sodium) plus dacarbazine in patients with advanced melanoma: the Oblimersen Melanoma Study Group. J Clin Oncol. 2006 Oct 10;24(29):4738-45. doi: 10.1200/JCO.2006.06.0483. Epub 2006 Sep 11.

    PMID: 16966688BACKGROUND

MeSH Terms

Conditions

MelanomaSkin Neoplasms

Interventions

DacarbazineoblimersenSodium Chloride

Condition Hierarchy (Ancestors)

Neuroendocrine TumorsNeuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasmsNeoplasms, Nerve TissueNevi and MelanomasNeoplasms by SiteSkin DiseasesSkin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

TriazenesOrganic ChemicalsImidazolesAzolesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsChloridesHydrochloric AcidChlorine CompoundsInorganic ChemicalsSodium Compounds

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 14, 2007

First Posted

August 21, 2007

Study Start

July 1, 2007

Primary Completion

May 1, 2011

Study Completion

May 1, 2011

Last Updated

November 7, 2011

Record last verified: 2009-04

Locations