CompletedPHASE1, PHASE2NCT00048737
Safety and Efficacy of 90Y Zevalin in Nonmyeloablative Transplantation for Lymphoid Malignancies
Studying Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement
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
- M.D. Anderson Cancer Center
- Principal Investigator
- Issa F. Khouri, MD, PA-CM.D. Anderson Cancer Center
- Intervention
- Zevalin Radioimmunotherapy(drug)
- Enrollment
- 70 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2002 – 2011
Study locations (1)
- MD Anderson Cancer Center, Houston, Texas, United States
Collaborators
Biogen
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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