Chidamide With ICE Regimen for Relapsed/Refractory Peripheral T Cell Lymphoma

NCT02856997 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2016-08-05

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy and safety of Chidamide with ICE regimen in patients with relapsed/refractory Peripheral T Cell lymphoma.

Conditions

  • Peripheral T Cell Lymphoma

Interventions

DRUG

Chidamide with ICE regimen

Chidamide and ICE regimen, dosage described in arm description

Sponsors & Collaborators

  • Yuankai Shi

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2019-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02856997 on ClinicalTrials.gov