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Brief Title: Phase I Study of BAY73-4506 in Chinese Patients With Advanced, Refractory Solid Tumors
Official Title: Uncontrolled, Open-label, Non-randomized, Phase 1 Study to Investigate the Pharmacokinetics, Safety, Tolerability, and Efficacy of BAY73-4506 in Chinese Patients With Advanced, Refractory Solid Tumors
Study ID: NCT01096030
Brief Summary: This will be an uncontrolled, open-label, non-randomized, phase I study. The primary objectives of this study are to define the pharmacokinetics (PK) and to evaluate the safety and tolerability of Regorafenib administered orally as a single agent in Chinese patients with advanced solid tumors. The secondary objectives are to evaluate tumor response of patients treated with Regorafenib.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, Shatin, N.T, Hong Kong
, Hong Kong, , Hong Kong
, Singapore, , Singapore
, Singapore, , Singapore
Name: Bayer Study Director
Affiliation: Bayer
Role: STUDY_DIRECTOR