CompletedPhase 2NCT00520208
Safety, Efficacy, & Pharmacokinetic Study of Tamibarotene to Treat Patients With Relapsed or Refractory APL
Studying Acute promyelocytic 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
- CytRx
- Principal Investigator
- Jorge Cortes, MDM.D. Anderson Cancer Center
- Intervention
- Tamibarotene(drug)
- Enrollment
- 15 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2007 – 2013
Study locations (2)
- Northwestern University, Chicago, Illinois, United States
- UT MD Anderson Cancer Center, Houston, Texas, United States
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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