- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00161668
Study Evaluating Mylotarg (Gemtuzumab Ozogamicin) in Usual Care
March 14, 2007 updated by: Wyeth is now a wholly owned subsidiary of Pfizer
Prospective Observational Study of Mylotarg (Gemtuzumab Ozogamicin) in Usual Care
This study is designed to assess the safety of Mylotarg therapy in routine practice.
Study Overview
Study Type
Observational
Enrollment
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Arizona
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Tucson, Arizona, United States, 85404
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California
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Berkely, California, United States, 94704
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Burbank, California, United States, 91505
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Concord, California, United States, 94520
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Loma Linda, California, United States, 92354
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Los Angeles, California, United States, 90095-1678
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San Francisco, California, United States, 94143
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Sylmar, California, United States, 91342
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Colorado
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Denver, Colorado, United States, 80218
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Florida
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Boynton Beach, Florida, United States, 33435
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Plantation, Florida, United States, 33324
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Stuart, Florida, United States, 34994
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Tamarac, Florida, United States, 33321
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Illinois
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Chicago, Illinois, United States, 60637
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Chicago, Illinois, United States, 60611
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Chicago, Illinois, United States, 60612-3838
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Chicago, Illinois, United States, 60612-7323
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Indiana
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Indianapolis, Indiana, United States, 46202
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Iowa
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Iowa City, Iowa, United States, 52242
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Kentucky
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Lexington, Kentucky, United States, 40536-0093
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Louisville, Kentucky, United States, 40202
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Louisiana
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Shrevport, Louisiana, United States, 71130-3932
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Michigan
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Ann Arbor, Michigan, United States, 48109-0999
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Grand Rapids, Michigan, United States, 49503
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Kalamazoo, Michigan, United States, 49048
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Kalamazoo, Michigan, United States, 49007-3731
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Missouri
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Columbia, Missouri, United States, 65203
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St. Louis, Missouri, United States, 63141
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New Jersey
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Neptune, New Jersey, United States, 07754
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New Mexico
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Albuquerque, New Mexico, United States, 87109
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New York
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Bronx, New York, United States, 10466
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Buffalo, New York, United States, 14263
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New Hyde Park, New York, United States, 11040
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New York, New York, United States, 10032
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New York, New York, United States, 10019
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Valhalla, New York, United States, 10595
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North Carolina
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Durham, North Carolina, United States, 27705
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Winston-Salem, North Carolina, United States, 27106
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North Dakota
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Bismarck, North Dakota, United States, 58501
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Ohio
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Akron, Ohio, United States, 44302
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Canton, Ohio, United States, 44718
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Cincinnati, Ohio, United States, 45236
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Cleveland, Ohio, United States, 44195
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Oklahoma
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Oklahoma City, Oklahoma, United States, 72112
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Oregon
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Portland, Oregon, United States, 97201
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Pennsylvania
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Hershey, Pennsylvania, United States, 17033-0850
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Philadelphia, Pennsylvania, United States, 19104
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Philadelphia, Pennsylvania, United States, 19107
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Pittsburgh, Pennsylvania, United States, 15224
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Tennessee
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Memphis, Tennessee, United States, 38120
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Nashville, Tennessee, United States, 37205
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Nashville, Tennessee, United States, 37232-5505
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Texas
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Houston, Texas, United States, 77030
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Temple, Texas, United States, 76508
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Virginia
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Arlington, Virginia, United States, 22205
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Richmond, Virginia, United States, 23298-0157
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West Virginia
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Charleston, West Virginia, United States, 25304
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Morgantown, West Virginia, United States, 26506-9162
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Wisconsin
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Appleton, Wisconsin, United States, 54911
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Treated by Mylotarg
- Provide ICF
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2001
Study Registration Dates
First Submitted
September 8, 2005
First Submitted That Met QC Criteria
September 11, 2005
First Posted (ESTIMATE)
September 12, 2005
Study Record Updates
Last Update Posted (ESTIMATE)
March 15, 2007
Last Update Submitted That Met QC Criteria
March 14, 2007
Last Verified
March 1, 2007
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0903X-100847
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.