NCT Number: NCT00037596
Study Evaluating Gemtuzumab Ozogamicin in Acute Myeloid Leukemia
The primary objectives are a) to establish the maximum tolerated dose of gemtuzumab ozogamicin in combination with cytarabine and b) to assess the safety of gemtuzumab ozogamicin when given concurrently with cytarabine.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Morphologic diagnosis of AML from bone marrow aspirate and biopsy
- Flow cytometry, performed at the study site, must demonstrate that the patient has AML that is CD33+, based on local laboratory criteria
- Age 18 years or older for relapsed or refractory patients for Phase I of this study
Exclusion criteria
- Patients with de novo AML of the M3 subtype
- AML following an antecedent hematologic disorder (myelodysplasia or myeloproliferation) of > 2 months duration
- AML secondary to exposure to chemotherapy or radiation
Treatment and study plan
cytarabine.
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Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Registry information
Official study title
A Dose Ranging Study of the Safety and Efficacy of Gemtuzumab Ozogamicin (GO) Given in Combination With Cytarabine in Relapsed or Refractory Patients and Alder De Novo Patients With Acute Myeloid Leukemia.
Important dates
- Study start
- 2000
- Primary completion
- 2003
- Study completion
- 2003
- First posted
- May 20, 2002
- Registry last updated
- Feb 13, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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