WithdrawnPHASE1, PHASE2NCT00676871
A Study to Evaluate the Safety, Tolerability, and Antitumor Activity of Continuous Intravenous Infusion of MEDI-538 in Adults With B-Cell Chronic Lymphocytic Leukemia (CLL)
Studying T-cell prolymphocytic leukemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- MedImmune LLC
- Principal Investigator
- Karen Kaucic, M.D.MedImmune LLC
- Intervention
- MEDI-538(drug)
- Enrollment
- 30 target
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2008 – 2011
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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