The study will evaluate the safety and efficacy of Patupilone in adult patients with advanced solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Novartis Investigative Site
Tokyo, Japan
Dose-limiting Toxicity
Time frame: 18 months
Safety and tolerability of patupilone assessed by CTCAE
Time frame: 18 months
Pharmacokinetic profile of patupilone
Time frame: 18 months
Anti-tumor activity of patupilone according to the RECIST guidelines
Time frame: 18 months
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