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Brief Title: An Extension Study Administering YM155 to Subjects Previously Enrolled in Another Protocol Administering YM155
Official Title: Phase II: An Open-Label Extension Study of 168-Hour Continuous Infusion of YM155 in Subjects Previously Enrolled in a Phase I or Phase II Protocol Administering YM155
Study ID: NCT00818480
Brief Summary: This protocol is open to subjects previously enrolled in and who had completed a Phase I or Phase II study administering YM155. Subjects who are receiving benefit from treatment with YM155 are eligible after completing the previous study.
Detailed Description: The main objective of the study is to continue to evaluate the safety and efficacy of YM155. Each subject will be treated at the dose he/she was receiving at the completion of his/her previous phase I or phase II YM155 study.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Institute for Drug Development, San Antonio, Texas, United States
South Texas Accelerated, San Antonio, Texas, United States
Huntsman Cancer Hospital, Salt Lake City, Utah, United States
Name: Sr. Medical Director
Affiliation: Astellas Pharma Global Development
Role: STUDY_DIRECTOR