Clinical Trials Logo

Clinical Trial Summary

To observe the efficacy and safety of Ruxolitinib and Etoposide combined with DDGP regimen ( cis-Platinum, Dexamethasone, Gemcitabine and Pegaspargase) in the first-line induction therapy of T cell lymphoma and NK/T cell lymphoma-associated hemophagocytic syndrome.


Clinical Trial Description

This is an open, one-arm, prospective clinical collaborative study. This study is aimed to observe the efficacy and safety of the new combined therapy of Ruxolitinib and Etoposide combined with DDGP regimen ( cis-Platinum, Dexamethasone, Gemcitabine and Pegaspargase) in the first-line induction therapy patients with primary central nervous system lymphoma. A total of 30 patients plan to participate in the study. The primary endpoint is objective remission rate (ORR) of hemophagocytic syndrome, and the secondary endpoints include progression-free survival (PFS) , objective remission rate (ORR) of lymphoma, overall survival (OS), and adverse events(ADR). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04999878
Study type Interventional
Source Zhengzhou University
Contact Mingzhi Zhang, Pro.Dr.
Phone 13838565629
Email Mingzhi_zhang@126.com
Status Recruiting
Phase Phase 4
Start date May 30, 2021
Completion date June 30, 2024

See also
  Status Clinical Trial Phase
Active, not recruiting NCT01494103 - Administration of Donor T Cells With the Caspase-9 Suicide Gene Phase 1
Recruiting NCT05882175 - Prospective Validation of the OHI Index
Not yet recruiting NCT05353179 - Study on Pharmacokinetics of Meperizumab Injection and NUCALA® in Healthy Male Volunteers Early Phase 1
Completed NCT02113917 - Children and Adult Hemophagocytic Syndrome (HLHa)
Not yet recruiting NCT04500886 - Evaluate the Efficacy and Safety of PEG-rhG-CSF in Patients With Hemophagocytic Syndrome N/A
Recruiting NCT05936086 - A Randomized Controlled Study of High-dose Cyclophosphamide Induction Therapy in Adult Patients With HLH N/A