Treatment Use Study for Advanced Melanoma.
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00584493|
Expanded Access Status : No longer available
First Posted : January 2, 2008
Last Update Posted : December 14, 2009
|First Submitted Date||December 21, 2007|
|First Posted Date||January 2, 2008|
|Last Update Posted Date||December 14, 2009|
|Brief Title||Treatment Use Study for Advanced Melanoma.|
|Brief Summary||The purpose of this study is to provide access to CP-675,206 for patients with advanced unresectable melanoma and who have the potential to gain benefit from this treatment and who are not eligible for participation in other CP-675,206 studies.|
|Detailed Description||This is an expanded access trial that canceled prior to enrolling patients.|
|Study Type||Expanded Access|
This is a single arm study. Patients will receive intravenous administration of CP-675,206 at a dose of 15 mg/kg on Day 1 of every 90-day cycle for up to 4 cycles. For purposes of treatment visits and scheduling, each cycle is defined as a 90 (± 4 day) period. Patients who discontinue treatment after 4 doses of CP-675,206 without disease progression and who subsequently experience disease progression more than 3 months after the last dose may receive 2 additional doses of CP-675,206 provided that they have not received other systemic therapy for their melanoma
Survival in this study will be monitored on all patients for up to 5 years from the date of first dose of CP-675,206.
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Expanded Access Status||No longer available|
|Contacts||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries||Not Provided|
|Removed Location Countries|
|Responsible Party||Director, Clinical Trial Disclosure Group, Pfizer Inc|
|Verification Date||December 2009|