Study Evaluating Mylotarg (Gemtuzumab Ozogamicin) in Usual Care


Last updated date
Study Location
Tucson, Arizona, 85404, United States


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Eligibility Criteria
The disease, disorder, syndrome, illness, or injury that is being studied.
Acute Myeloid Leukemia
Females and Males
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18-65 years
Inclusion Criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

- Treated by Mylotarg

- Provide ICF


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Advanced Information
Descriptive Information
Brief Title Study Evaluating Mylotarg (Gemtuzumab Ozogamicin) in Usual Care
Official Title Prospective Observational Study of Mylotarg (Gemtuzumab Ozogamicin) in Usual Care
Brief Summary This study is designed to assess the safety of Mylotarg therapy in routine practice.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
Condition Acute Myeloid Leukemia
Intervention Drug: Mylotarg
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Recruitment Information
Recruitment Status Completed
 (submitted: September 11, 2005)
Original Enrollment Same as current
Study Completion Date Not Provided
Primary Completion Date Not Provided
Eligibility Criteria

Inclusion Criteria:

  • Treated by Mylotarg
  • Provide ICF
Sexes Eligible for Study:All
Ages 18 Years to 65 Years   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
Administrative Information
NCT Number NCT00161668
Other Study ID Numbers 0903X-100847
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Not Provided
Study Sponsor Wyeth is now a wholly owned subsidiary of Pfizer
Collaborators Not Provided
Study Director:Medical MonitorWyeth is now a wholly owned subsidiary of Pfizer
PRS Account Wyeth is now a wholly owned subsidiary of Pfizer
Verification Date March 2007