![]() |
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
Sponsored by: |
Astellas Pharma Inc |
---|---|
Information provided by: | Astellas Pharma Inc |
ClinicalTrials.gov Identifier: | NCT00818480 |
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.
Condition | Intervention | Phase |
---|---|---|
Prostate Cancer Melanoma Non-Hodgkin's Lymphoma |
Drug: YM155 |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Single Group Assignment, Safety/Efficacy Study |
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 |
Estimated Enrollment: | 100 |
Study Start Date: | February 2006 |
Estimated Study Completion Date: | December 2010 |
Estimated Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1. YM155: Experimental |
Drug: YM155
continuous infusion
|
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.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Texas | |
San Antonio, Texas, United States, 78229 | |
United States, Utah | |
Salt Lake City, Utah, United States, 84112 |
Study Director: | Use Central Contact | Astellas Pharma US, Inc. |
Responsible Party: | Astellas Pharma US, Inc ( Sr Manager Clinical Trial Registry ) |
Study ID Numbers: | 155-CL-101 |
Study First Received: | January 6, 2009 |
Last Updated: | January 6, 2009 |
ClinicalTrials.gov Identifier: | NCT00818480 |
Health Authority: | United States: Food and Drug Administration |
prostate cancer melanoma lymphoma YM155 |
Immunoproliferative Disorders Prostatic Diseases Genital Neoplasms, Male Lymphoma, small cleaved-cell, diffuse Urogenital Neoplasms Genital Diseases, Male Melanoma Neuroendocrine Tumors Lymphatic Diseases |
Neuroectodermal Tumors Neoplasms, Germ Cell and Embryonal Nevus, Pigmented Neuroepithelioma Nevus Lymphoma, Non-Hodgkin Lymphoproliferative Disorders Lymphoma Prostatic Neoplasms |
Neoplasms Neoplasms by Site Neoplasms by Histologic Type |
Immune System Diseases Neoplasms, Nerve Tissue Nevi and Melanomas |