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Clinical Trial Summary

This is a multicenter prospective single arm phase II study. The purpose of this study is to evaluate the safety and efficiency of azacytidine combined with CAOLD Regimen in the treatment of relapsed/refractory angioimmunoblastic T-cell lymphoma.


Clinical Trial Description

The investigators will evaluate response rate, progression free survival (PFS), overall survival (OS), and toxicity of azacytidine combined with CAOLD Regimen in relapsed/refractory angioimmunoblastic T-cell lymphoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06176027
Study type Interventional
Source Navy General Hospital, Beijing
Contact Liren Qian, PhD
Phone +861066957676
Email qlr2007@126.com
Status Recruiting
Phase Phase 1/Phase 2
Start date August 1, 2024
Completion date September 1, 2030

See also
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Active, not recruiting NCT03278782 - Study of Pembrolizumab (MK-3475) in Combination With Romidepsin Phase 1/Phase 2
Terminated NCT03075553 - Nivolumab in Treating Patients With Relapsed or Refractory Peripheral T-cell Lymphoma Phase 2
Withdrawn NCT04795869 - Brentuximab Vedotin and Pembrolizumab in Treating Patients With Recurrent Peripheral T-Cell Lymphoma Phase 2
Active, not recruiting NCT03598998 - Pembrolizumab and Pralatrexate in Treating Patients With Relapsed or Refractory Peripheral T-Cell Lymphomas Phase 1/Phase 2
Recruiting NCT03017820 - VSV-hIFNbeta-NIS in Treating Patients With Relapsed or Refractory Multiple Myeloma, Acute Myeloid Leukemia or Lymphoma Phase 1