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NCT06652139Not yet recruitingPhase 2

Selinexor Combined With BEAM for ASCT in R/R DLBCL With MYC Positive

A Single-center, Randomized Controlled Clinical Study of Selinexor Combined With BEAM as a Preconditioning Regimen for ASCT in Relapsed and Refractory Diffuse Large B-cell Lymphoma With MYC Positive

Source: ClinicalTrials.gov · Last updated 22 Oct 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To evaluate the efficacy and safety of selinexor combined with BEAM pretreatment regimen in ASCT of recurrent and refractory DLBCL patients with immunohistochemical positive for MYC

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
82 (estimated)
First submitted
21 Oct 2024
Start date
1 Nov 2024
Primary completion date
1 Nov 2026
Lead sponsor
Ruijin Hospital
NCT number
NCT06652139

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 82
  • From 1 Nov 2024 to the primary completion date, 1 Nov 2026
  • No sites listed in no 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 design.

Who cannot take part

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

Prior treatment

  • Previously received autologous hematopoietic stem cell transplantation;
  • Previous treatment with selinexor;
  • Other concurrent and uncontrolled medical conditions considered by the investigator would affect the patient's participation in the study;

Other illness

  • Suffering from serious complications or severe infection;
  • A history of other malignant tumors within 5 years, excluding early tumors treated for curative purposes;
  • Patients with uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, serious infectious diseases, etc.;
  • HBsAg, HCV or HIV positive. Positive HBV and HCV serology is allowed, but DNA/RNA testing must be negative;
  • Psychiatric patients or other patients known or suspected to be unable to fully comply with the study protocol;

Lab values

  • Left ventricular ejection fraction ≦ 50%;
  • Laboratory test value during screening;
    • ① Neutrophils <1.5×109/L; Platelet <75×109/L;
    • ② Bilirubin was 1.5 times higher than the normal upper limit, transaminase was 2.5 times higher than the normal upper limit;
    • ③ The creatinine level is higher than 1.5 times the upper limit of normal value;

Other

  • Central nervous system lymphoma was excluded;
  • Pregnant or lactating women;
  • The researcher judged that the patients were not suitable for this study.

Who the study is looking for

  • According to world Health Organization (WHO) classification of disease, diffuse large B-cell lymphoma was confirmed by histology, CR or PR after second-line and above treatment;
  • The subjects tested positive for MYC in primary or pre-transplant lymphoma lesions;
  • 18≤ age ≤65 years old, male or female;
  • ECOG score 0-2;
  • No serious organic lesions in the main organs, meeting the requirements of the following laboratory examination indicators (conducted within 7 days before treatment) :
    • White blood cell count ≥3.0×109/L, absolute neutrophil count ≥1.5×109/L, Hemoglobin ≥90g/L, platelet ≥75×109/L;
    • Total bilirubin ≤1.5× upper normal value (ULN);
    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5× ULN; Bilirubin ≤1.5× ULN
    • Creatinine clearance was 44-133 mmol/L;
  • No cardiac dysfunction;
  • Life expectancy over 3 months;
  • The subject or his/her legal representative must provide written informed consent prior to conducting a special study examination or procedure.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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