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RecruitingNCT06176027

Azacytidine Plus CAOLD Regimen in Relapsed/Refractory Peripheral T-Cell Lymphomas

Therapeutic Effect of Chemotherapy Azacytidine Plus CAOLD Regimen on Patients With Relapsed/Refractory Peripheral T-Cell Lymphomas

Status
Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
52 (estimated)
Sponsor
Navy General Hospital, Beijing · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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 peripheral t-cell lymphomas.

Detailed 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 peripheral t-cell lymphomas.

Conditions

Interventions

TypeNameDescription
DRUGAzacytidine plus CAOLD regimenPatients were treated by Azacytidine(75 mg/m2 on days 1-7) plus CAOLD regimen (cyclophosphamide 400mg/m2 qd d1; cytarabine 30mg/m2 qd d1-d4; vindesine 2mg/m2 qd d1; pegaspargase 2500iu/m2 qd d2; dexamethasone 7.5mg/m2 qd d1-d5)

Timeline

Start date
2024-10-01
Primary completion
2028-09-01
Completion
2030-09-01
First posted
2023-12-19
Last updated
2024-10-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06176027. Inclusion in this directory is not an endorsement.

Azacytidine Plus CAOLD Regimen in Relapsed/Refractory Peripheral T-Cell Lymphomas (NCT06176027) · Clinical Trials Directory