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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
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:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, Hong Kong, , Hong Kong
, Hong Kong, , Hong Kong
, Jogjakarta, , Indonesia
, Kuala Lumpur, , Malaysia
, Kueishan, , Taiwan
, Taipei, , Taiwan
, Taipei, , Taiwan
, Bangkok, , Thailand
, Bangkok, , Thailand
Name: Clinical Trials
Affiliation: Hoffmann-La Roche
Role: STUDY_CHAIR