58
Participants
Start Date
November 30, 2009
Primary Completion Date
June 30, 2011
Study Completion Date
June 30, 2011
Ixabepilone
Vial, Injection, Intravenous (IV), 40 mg/m\^2, Every 21 days, Up to 8 cycles or until disease progression or intolerable toxicity. Additional treatment was given in agreement by both the investigator and sponsor. Ixabepilone 40 mg/m\^2 was administered as a 3-hour IV infusion on Day 1 of each 21-day (3 week) cycle provided the participant met the retreatment criteria.
Local Institution, Taipei
Local Institution, Taoyuan Hsien
Local Institution, Singapore
Local Institution, Sunto-Gun
Local Institution, Nagoya
Local Institution, Hong Kong
Local Institution, Seoul
Local Institution, Seoul
Local Institution, Seoul
Lead Sponsor
R-Pharm
INDUSTRY