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Clinical Trial Summary

To determine the maximum tolerated dose (MTD), if present, and dose schedule of ruxolitinib in combination with L-ASP, vincristine, and prednisone (LVP) in patients with relapsed-and-refractory (R/R) early T precursor acute lymphocytic leukemia (ETP-ALL). Once determined, the purpose of this study will be to determine the efficacy of ruxolitinib in combination with LVP in patients with R/R ETP-ALL.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03613428
Study type Interventional
Source Sichuan University
Contact Jie Ji, MD
Phone 86-18980605802
Email jieji@scu.edu.cn
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date December 1, 2018
Completion date March 30, 2021

See also
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