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Completed

NCT Number: NCT04661943

Maintenance Therapy of Chidamide in Patients With HBV Positive Diffuse Large B-cell Lymphoma

A phase II,single arm,open-label study to assess Maintenance Therapy of Chidamide in Patients With Hepatitis B Virus(HBV)Positive Diffuse Large B-cell Lymphoma with complete response after completion of prior chemotherapy

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Bethune Hospital of Jilin University

Changchun, Jilin, 130021, China

About this study

Objective to evaluate the efficacy and safety of maintenance therapy with Chidamide in patients With Hepatitis B Virus(HBV)Positive Diffuse Large B-cell Lymphoma(DLBCL) with complete response after completion of prior chemotherapy, so as to provide the basis for the application of Chidamide in HBV positive DLBCL

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • histopathology confirmed DLBCL,with chronic hepatitis B before treatment
  • After systemic treatment, complete response has been achieved and complete response lasted within 1year before enrollment
  • The expected chemotherapy was completed and the laboratory indexes returned to normal
  • The absolute value of neutrophil ≥ 1.5 × 10 9 / L, platelet count≥ 90 × 10 9 / L, hemoglobin level≥ 90 g / L
  • Patients who cannot undergo hematopoietic stem cell transplantation for various reasons
  • 18-75 years old, both male and female
  • ECOG PS 0-1
  • Body weight: male 67 ± 20 kg (47-87 kg), female 55 ± 20 kg (35-75 kg)
  • expected survival time ≥3 months
  • Voluntary written informed consent prior to trail screening

Exclusion criteria

  • Pregnant and lactating women and women of childbearing age who are unwilling to take contraceptive measures
  • Patients with prolonged QTc interval (male > 450ms, female > 470ms), ventricular tachycardia (VT), atrial fibrillation (AF), heart block, myocardial infarction (MI) within 1 year, congestive heart failure (CHF), and coronary heart disease with symptoms requiring drug treatment
  • B-ultrasound showed that the width of the fluid dark area in the pericardial cavity was ≥ 10 mm at the end of diastolic period
  • Patients with previous or planned organ transplantation
  • Patients receiving symptomatic treatment for early myelotoxicity within 7 days before enrollment
  • HBV nucleic acid quantitation > 103 IU / ml
  • Patients with active bleeding
  • Patients with thrombosis, embolism, cerebral hemorrhage, cerebral infarction and other this kind of diseases or medical history
  • Patients with active infection or persistent fever within 14 days before enrollment
  • less than 6 weeks after major organ surgery
  • Abnormal liver function [total bilirubin > 1.5 times of the upper limit of normal value; ALT / AST > 2.5 times of upper limit of normal value for patients without liver metastasis ; ALT / AST > 5 times of upper limit of normal value for patients with liver metastasis ], abnormal renal function (serum creatinine > 1.5 times of upper limit of normal value)
  • Mental disorders/Those who cannot obtain informed consent
  • Patients with drug abuse and long-term alcohol abuse that affect evaluation
  • The investigator determined not suitable to participate in this study

Treatment and study plan

Tucidinostat

Drug

Tucidinostat Specification: 5mg / tablet. Dosage: oral, 20 mg (3 tablets) each time, twice a week, with the interval of no less than 3 days (such as Monday and Thursday, Tuesday, Friday, Wednesday and Saturday, etc.)

Other names: Chidamide,CS055,HBI-8000

Primary outcomes

  1. Progression-free survival

    Time frame: 6months

    Progression-free survival(by IWC)

Secondary outcomes

  1. Overall survival

    Time frame: 12months

    Overall survival

Sponsors and collaborators

Lead sponsor

Ou Bai, MD/PHD

Other

Registry information

Important dates

Study start
2017
Primary completion
2024
Study completion
2024
First posted
Dec 10, 2020
Registry last updated
Mar 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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