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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00257205
Other study ID # A3671009
Secondary ID
Status Completed
Phase Phase 3
First received November 18, 2005
Last updated June 25, 2012
Start date March 2006
Est. completion date August 2010

Study information

Verified date June 2012
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a Phase 3, multi-national, open-label, 2-arm randomized study in patients with surgically incurable metastatic melanoma who have received no prior chemotherapy, or biochemotherapy for the treatment of metastatic disease. The primary objective of this trial is to compare overall survival for patients with advanced melanoma who are randomized to receive CP-675,206 with that of patients who are randomized to receive either dacarbazine or temozolomide (investigator choice)


Recruitment information / eligibility

Status Completed
Enrollment 655
Est. completion date August 2010
Est. primary completion date August 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Surgically incurable melanoma, either Stage IV or IIIC with N3 status for regional lymph nodes and in-transit or satellite lesions.

- Serum lactic acid dehydrogenase (LDH) <= 2 x ULN

- ECOG performance status of 0 or 1

Exclusion Criteria:

- Received any systemic therapy for metastatic melanoma except post-surgical adjuvant treatment with cytokines (eg, alpha-interferon or GM-CSF) or with vaccines after complete resection of melanoma.

- History of brain metastases

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
dacarbazine
decarbazine 1000 mg/m2 IV Q 21 days x 12
CP-675,206
CP-675,206 15 mg/kg IV Q 90 days x 4
temozolomide
temozolomide 200 mg/m2 orally on Days 1-5 every 28 days x 12

Locations

Country Name City State
Argentina Research Site Ciudad de Buenos Aires Buenos Aires
Australia Research Site Adelaide South Australia
Australia Research Site East Melbourne Victoria
Australia Research Site Launceston Tasmania
Australia Research Site Waratah New South Wales
Australia Research Site Westmead New South Wales
Australia Research Site Woolloongabba Queensland
Austria Research Site Wien
Belgium Research Site Brussel
Belgium Research Site Leuven
Belgium Research Site Namur
Belgium Research Site Roeselare
Belgium Research Site Turnhout
Belgium Research Site Wilrijk
Belgium Research Site Yvoir
Canada Research Site Calgary Alberta
Canada Research Site Edmonton Alberta
Canada Research Site Hamilton Ontario
Canada Research Site London Ontario
Canada Research Site Montreal Quebec
Canada Research Site Quebec
Canada Research Site Toronto Ontario
Canada Research Site Toronto Ontario
Canada Research Site Vancouver British Columbia
Canada Research Site Victoria British Columbia
Canada Research Site Windsor Ontario
Canada Research Site Windsor Ontario
Canada Research Site Winnipeg Manitoba
France Research Site Besancon
France Research Site Bordeaux
France Research Site Boulogne
France Research Site Caen
France Research Site Lille
France Research Site Marseille
France Research Site Montpellier Cedex 05
France Research Site Nantes Cedex 1
France Research Site Paris
Germany Research Site Berlin
Germany Research Site Frankfurt
Germany Research Site Hannover
Germany Research Site Kiel
Germany Research Site Tuebingen
Greece Research Site Athens
Israel Research Site Jerusalem
Israel Research Site Tel Aviv
Israel Research Site Tel Hashomer
Italy Research Site Genova
Italy Research Site Milano
Italy Research Site Napoli
Italy Research Site Padova
Italy Research Site Roma
Italy Research Site Siena
Mexico Research Site Mexico DF
Mexico Research Site Mexico DF
Netherlands Research Site Amsterdam NH
Netherlands Research Site Groningen GR
Netherlands Research Site Leiden ZH
Netherlands Research Site Nijmegen
Poland Research Site Bialystok
Poland Research Site Krakow
Poland Research Site Lubin
Poland Research Site Poznan
Poland Research Site Warszawa
Russian Federation Research Site Moscow
Russian Federation Research Site Obninsk Kaluga Region
Russian Federation Research Site St. Petersburg
Slovakia Research Site Bratislava
South Africa Research Site Cape Town
South Africa Research Site Pretoria
Spain Research Site Barcelona
Spain Research Site Hospitalet de Llobregat Barcelona
Spain Research Site Madrid
Spain Research Site Oviedo Asturias
Spain Research Site Palma de Mallorca Islas Baleares
Spain Research Site Pamplona Navarra
Spain Research Site Santander Cantabria
Spain Research Site Zaragoza
Sweden Research Site Goteborg
Sweden Research Site Lund
Switzerland Research Site Zurich
United Kingdom Research Site London
United Kingdom Research Site Manchester
United Kingdom Research Site Newcastle upon Tyne
United Kingdom Research Site Newcastle Upon Tyne
United Kingdom Research Site Northwood Middlesex
United Kingdom Research Site Sutton Surrey
United Kingdom Research Site Truro Cornwall
United Kingdom Research Site Wolverhampton
United States Research Site Albany New York
United States Research Site Aurora Colorado
United States Research Site Bakersfield California
United States Research Site Baltimore Maryland
United States Research Site Beech Grove Indiana
United States Research Site Bethlehem Pennsylvania
United States Research Site Boynton Beach Florida
United States Research Site Canton Ohio
United States Research Site Chapel Hill North Carolina
United States Research Site Charlotte North Carolina
United States Research Site Charlotte North Carolina
United States Research Site Columbus Ohio
United States Research Site Corona California
United States Research Site Creve Coeur Missouri
United States Research Site Dallas Texas
United States Research Site Dover Ohio
United States Research Site Federal Way Washington
United States Research Site Fullerton California
United States Research Site Glendora California
United States Research Site Henderson Nevada
United States Research Site Henderson Nevada
United States Research Site Huntington Beach California
United States Research Site Huntsville Alabama
United States Research Site Indianapolis Indiana
United States Research Site Indianapolis Indiana
United States Research Site Lake Worth Florida
United States Research Site Lakewood Washington
United States Research Site Las Vegas Nevada
United States Research Site Las Vegas Nevada
United States Research Site Las Vegas Nevada
United States Research Site Las Vegas Nevada
United States Research Site Little Rock Arkansas
United States Research Site Long Beach California
United States Research Site Los Alamitos California
United States Research Site Los Angeles California
United States Research Site Los Angeles California
United States Research Site Mobile Alabama
United States Research Site Morristown New Jersey
United States Research Site New York New York
United States Research Site Omaha Nebraska
United States Research Site Oxnard California
United States Research Site Pasadena California
United States Research Site Pittsburgh Pennsylvania
United States Research Site Pomona California
United States Research Site Rancho Cucamonga California
United States Research Site Salt Lake City Utah
United States Research Site Santa Barbara California
United States Research Site Santa Maria California
United States Research Site Scottsdale Arizona
United States Research Site St Louis Missouri
United States Research Site St. Louis Missouri
United States Research Site St. Peters Missouri
United States Research Site Stamford Connecticut
United States Research Site Tacoma Washington
United States Research Site West Covina California
United States Research Site Zion Illinois

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Austria,  Belgium,  Canada,  France,  Germany,  Greece,  Israel,  Italy,  Mexico,  Netherlands,  Poland,  Russian Federation,  Slovakia,  South Africa,  Spain,  Sweden,  Switzerland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival August 2010 No
Secondary adverse events 1 year No
Secondary PFS at 6 months 6 months No
Secondary objective tumor response 1 year No
Secondary Durable response 6 months No
Secondary pharmacokinetics endpoints 15 months No
Secondary pharmacogenomic endpoints 1 year No
Secondary HQol 1 year No
Secondary healthcare resource utilization and loss of productivity 1 year No
Secondary human antihuman antibody response for patients in Arm A 15 months No
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