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view post Posted on 5/5/2012, 23:22

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An Investigational Drug, PF-02341066 Is Being Studied Versus Standard Of Care In Patients With Advanced Non-Small Cell Lung Cancer With A Specific Gene Profile Involving The Anaplastic Lymphoma Kinase (ALK) Gene
Trial Description

Summary

This is a Phase 3 trial comparing the safety and anti-tumor activity of PF-02341066 versus pemetrexed or docetaxel in patients with advanced non-small lung cancer with specific gene profile involving the ALK gene after failure of one previous chemotherapy regimen that included one platinum drug.

Eligibility Criteria

Inclusion Criteria:

histologically or cytologically proven diagnosis of non-small cell lung cancer

positive for the ALK fusion gene (test provided by a central laboratory)

must have had disease progression after only one prior chemotherapy and that regimen but must have included one platinum drug

tumors must be measurable

Exclusion Criteria:

prior treatment with PF-02341066

current treatment in another clinical trial

Trial Contact Information

Trial Lead Organizations/Sponsors

Pfizer Incorporated
Pfizer CT.gov Call Center Study Director

Pfizer CT.gov Call Center Ph: 1-800-718-1021

Pfizer Oncology Clinical Trial Information Service Ph: 1-877-369-9753
Email: [email protected]

Trial Sites


U.S.A.
Washington
Seattle

Pfizer Investigational Site
Australia
New South Wales
Camperdown
Pfizer Investigational Site
South Australia
Adelaide
Pfizer Investigational Site
Victoria
Bentleigh
Pfizer Investigational Site
East Melbourne
Pfizer Investigational Site
Fitzroy
Pfizer Investigational Site
Footscray
Pfizer Investigational Site
Frankston
Pfizer Investigational Site
Parkville
Pfizer Investigational Site
Brazil
Sao Paulo
Barretos
Pfizer Investigational Site
Jau
Pfizer Investigational Site
Sao Paulo
Pfizer Investigational Site
Canada
Quebec
Montreal
Pfizer Investigational Site
China
Beijing
Pfizer Investigational Site
Shanghai
Pfizer Investigational Site
France
Villejuif
Pfizer Investigational Site
Germany
Dresden
Pfizer Investigational Site
Essen
Pfizer Investigational Site
Grosshansdorf
Pfizer Investigational Site
Hamburg
Pfizer Investigational Site
Heidelberg
Pfizer Investigational Site
Koeln
Pfizer Investigational Site
Muenchen
Pfizer Investigational Site
Oldenburg
Pfizer Investigational Site
Wiesbaden
Pfizer Investigational Site
Hong Kong
Hong Kong
Pfizer Investigational Site
Shatin, New Territories
Pfizer Investigational Site
Tuen Mun, New Territories
Pfizer Investigational Site
Hungary
Budapest
Pfizer Investigational Site
Szekesfehervar
Pfizer Investigational Site
Italy
Avellino
Pfizer Investigational Site
Lido di Camaiore (LU)
Pfizer Investigational Site
Lucca
Pfizer Investigational Site
Milano
Pfizer Investigational Site
Monza
Pfizer Investigational Site
Torino
Pfizer Investigational Site
Japan
Tokyo
Pfizer Investigational Site
Netherlands
Groningen
Pfizer Investigational Site
Republic of Korea
Seoul
Pfizer Investigational Site
Russia
Saint-Peterburg
Pfizer Investigational Site
Saint-Petersburg
Pfizer Investigational Site
St. Petersburg
Pfizer Investigational Site
Spain
Barcelona
Pfizer Investigational Site
L'hospitalet de Llobregat
Pfizer Investigational Site
Sabadell
Pfizer Investigational Site
Sevilla
Pfizer Investigational Site
United Kingdom
London
Pfizer Investigational Site
Manchester
Pfizer Investigational Site
Sutton
Pfizer Investigational Site

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00932893
Information obtained from ClinicalTrials.gov on April 17, 2012

Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain the same text. Minor changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should be directed to ClinicalTrials.gov.
 
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view post Posted on 7/5/2012, 01:10

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