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Spots Global Cancer Trial Database for A Study of Capecitabine (Xeloda) as First-Line Chemotherapy in Participants With Metastatic Nasopharyngeal Cancer

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Trial Identification

Brief Title: A Study of Capecitabine (Xeloda) as First-Line Chemotherapy in Participants With Metastatic Nasopharyngeal Cancer

Official Title: A Multi-Center Phase II Trial of Capecitabine (Xeloda) in Combination With Cisplatin as First Line Chemotherapy in Patients With Metastatic Nasopharyngeal Carcinoma

Study ID: NCT02608073

Study Description

Brief Summary: This study will evaluate the efficacy, safety, tolerability, and effect on quality of life of oral capecitabine in combination with intravenous (IV) cisplatin in participants with metastatic nasopharyngeal cancer. Participants will receive up to 8 cycles of capecitabine treatment, and cisplatin will be administered on the first day of each cycle. The anticipated time on study treatment is up to 24 weeks, and the target sample size is 44 individuals.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

, Hong Kong, , Hong Kong

, Hong Kong, , Hong Kong

, Jogjakarta, , Indonesia

, Kuala Lumpur, , Malaysia

, Kueishan, , Taiwan

, Taipei, , Taiwan

, Taipei, , Taiwan

, Bangkok, , Thailand

, Bangkok, , Thailand

Contact Details

Name: Clinical Trials

Affiliation: Hoffmann-La Roche

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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