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Spots Global Cancer Trial Database for An Extension Study Administering YM155 to Subjects Previously Enrolled in Another Protocol Administering YM155

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Trial Identification

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

Interventions

YM155

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Sr. Medical Director

Affiliation: Astellas Pharma Global Development

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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