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A Randomized Phase II Study of Concurrent Cisplatin-radiotherapy With or Without Neoadjuvant Chemotherapy Using Taxotere and Cisplatin in Advanced Nasopharyngeal Carcinoma (NPC)
Primary objective: To assess and compare the toxicities of patients with advanced NPC treated with concurrent cisplatin-radiotherapy with or without neoadjuvant Taxotere (docetaxel) and cisplatin. Secondary objective: To assess tumor control and survival
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Sanofi-Aventis
Hong Kong, Hong Kong
Start Date
December 1, 2002
Primary Completion Date
March 1, 2010
Completion Date
March 1, 2010
Last Updated
November 17, 2010
61
ACTUAL participants
Docetaxel
DRUG
Cisplatin
DRUG
Lead Sponsor
Sanofi
NCT07326358
NCT05807880
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 ConditionsNCT00342147