CompletedPhase 2NCT01869114
Sirolimus and Azacitidine in Treating Patients With High Risk Myelodysplastic Syndrome or Acute Myeloid Leukemia That is Recurrent or Not Eligible for Intensive Chemotherapy
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
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
- Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
- Principal Investigator
- Margaret Kasner, MDSidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
- Intervention
- Sirolimus(drug)
- Enrollment
- 57 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2024
Study locations (5)
- Jefferson Health NJ Division (Kennedy Hospital), Sewell, New Jersey, United States
- Abington Hospital - Jefferson Health, Abington, Pennsylvania, United States
- Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University, Philadelphia, Pennsylvania, United States
- Jefferson Health, Aria Hospital, Philadelphia, Pennsylvania, United States
- Jefferson Health, Methodist Hospital, Philadelphia, Pennsylvania, 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.
Open NCT01869114 on ClinicalTrials.govOther trials for Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
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