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Brief Title: A Phase I Study of Oral BGJ398 in Asian Patients
Official Title: A Phase I Study of Oral BGJ398 in Asian Patients With Advanced Solid Tumor Having Alterations of the FGF-R Pathway
Study ID: NCT01697605
Brief Summary: This study will evaluate safety and tolerability to determine the Maximum tolerated dose (MTD) and/or Recommended dose (RD).
Detailed Description: This is a multi-center, open label, dose finding, phase I study of oral single agent BGJ398, administered on a continuous once and/or twice daily schedule.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Novartis Investigative Site, Guangzhou, Guangdong, China
Novartis Investigative Site, Chengdu, Sichuan, China
Novartis Investigative Site, Guangzhou, , China
Nagoya University Hospital, Nagoya-city, Aichi, Japan
National Cancer Center Hospital East (NCEE), Kashiwa, Chiba, Japan
Novartis Investigative Site, Kobe-shi, Hyogo, Japan
Novartis Investigative Site, Sayama, Osaka, Japan
Shizuoka Cancer Center, Sunto-gun, Shizuoka, Japan
Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR