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NCT07507318RecruitingPhase 2

Chidamide Maintenance for MRD-Positive Double-Expressor DLBCL in First Complete Remission

A Prospective, Multicenter, Single-Arm, Open-Label Phase 2 Study of Chidamide Maintenance in Patients With Newly Diagnosed Double-Expressor Diffuse Large B-Cell Lymphoma Who Achieve Complete Response After Induction Therapy But Remain ctDNA MRD-Positive

Source: ClinicalTrials.gov · Last updated 18 Jun 2026

Brief summary (registry, in English)

This is a prospective, multicenter, single-arm, open-label phase 2 study designed to evaluate the efficacy and safety of chidamide maintenance in adults with newly diagnosed double-expressor diffuse large B-cell lymphoma (DLBCL) who achieve complete response after induction therapy but remain ctDNA minimal residual disease (MRD)-positive. Eligible participants will receive oral chidamide 20 mg on Days 1, 4, 8, and 11 of each 21-day cycle. ctDNA MRD will be assessed every 12 weeks. Treatment will continue until two consecutive MRD-negative assessments, disease progression, intolerable toxicity, withdrawal of consent, or completion of 2 years of maintenance. The primary objectives are to evaluate ctDNA MRD negativity and 2-year progression-free survival. Secondary objectives include event-free survival, overall survival, and safety.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
69 (estimated)
First submitted
27 Mar 2026
Start date
16 Jun 2026
Primary completion date
30 Jun 2029
Lead sponsor
Rong Tao
NCT number
NCT07507318

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 69
  • From 16 Jun 2026 to the primary completion date, 30 Jun 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior organ transplantation.
  • Major organ surgery within 6 weeks before screening.
  • Drug abuse or chronic alcohol abuse that may interfere with study evaluation.
  • Requirement for ongoing treatment with strong or moderate CYP3A inhibitors or inducers; patients exposed to these agents within 7 days before first study dose, or within fewer than 5 half-lives, are not eligible.

Other illness

  • Failure to achieve complete response after initial induction therapy.
  • Uncontrolled coagulopathy or active bleeding.
  • Active hepatitis B not meeting protocol-defined virologic criteria for enrollment; patients with positive HBsAg or positive HBcAb require HBV DNA testing and must meet protocol-specified thresholds.
  • HIV infection.
  • Ongoing antitumor therapy for lymphoma or another malignancy.
  • Psychiatric illness or any condition resulting in inability to comply with the protocol.
  • Inability to swallow capsules or clinically significant gastrointestinal disorders that may affect drug absorption, including malabsorption syndrome, bariatric surgery, inflammatory bowel disease, or partial/complete bowel obstruction.
  • Any other uncontrolled medical condition that, in the investigator's judgment, may compromise safety, interfere with oral drug absorption or metabolism, or place the participant at excessive risk.

Lab values

  • Uncontrolled cardiovascular or cerebrovascular disease, including left ventricular ejection fraction \<50%, connective tissue disease, or severe active infection.
  • Screening laboratory abnormalities not attributable to lymphoma, including: neutrophil count \<1.5 x 10\^9/L; platelet count \<80 x 10\^9/L (or \<50 x 10\^9/L in patients with bone marrow involvement); total bilirubin \>1.5 x upper limit of normal; ALT/AST \>2.5 x upper limit of normal, or \>5 x upper limit of normal in patients with hepatic involvement; serum creatinine \>1.5 x upper limit of normal.

Who the study is looking for

  • Histologically confirmed diffuse large B-cell lymphoma, CD20-positive.
  • Double-expressor lymphoma confirmed by pathology, defined as MYC expression \>=40% and BCL2 expression \>=50% by immunohistochemistry.
  • Complete response after initial induction therapy.
  • Age \>=18 and \<=80 years.
  • ECOG performance status 0-2.
  • No prior history of malignant tumor and no concurrent malignancy.
  • International Prognostic Index (IPI) score \>1.
  • ctDNA MRD-positive at screening/enrollment.
  • Life expectancy of at least 6 months, in the opinion of the investigator.
  • Written informed consent provided before any study-specific procedure.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan University Shanghai Cancer Center
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.