CompletedEarly Phase 1NCT01184885
A Pilot Study to Determine the Safety and Tolerability of Sirolimus Given With Hyper-CVAD Chemotherapy
Studying Acute lymphoblastic 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
- Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
- Principal Investigator
- Margaret Kasner, MDThomas Jefferson University
- Intervention
- Hyper-CVAD(drug)
- Enrollment
- 7 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2010 – 2013
Study locations (2)
- University of Pennsylvania, Philadelphia, Pennsylvania, United States
- Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Collaborators
American Society of Clinical Oncology
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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