CompletedPhase 1NCT00981240
Dose Escalation, Safety and Pharmacokinetic Study of SAR103168 in Patients Refractory/ Relapsed Acute Leukemias or High-risk Myelodysplastic Syndromes
Studying Acute myeloid 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
- Sanofi
- Principal Investigator
- Farhad Ravandi-Kashani, MDM.D. Anderson Cancer Center, Houston, Texas
- Intervention
- SAR103168(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2009 – 2012
Study locations (3)
- Sanofi-Aventis Investigational Site Number 840003, Atlanta, Georgia, United States
- Sanofi-Aventis Investigational Site Number 840002, New York, New York, United States
- Sanofi-Aventis Investigational Site Number 840001, 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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