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NCT06514768RecruitingEarly phase 1

JY231 (JY231) Injection for the Treatment of B-cell Acute Lymphoblastic Leukemia (B-ALL)

Early Exploratory Clinical Study on the Safety, Tolerability and Preliminary Efficacy of JY231 Injection in the Treatment of Acute B Lymphoblastic Leukemia

Source: ClinicalTrials.gov · Last updated 6 Jan 2026

Brief summary (registry, in English)

Early exploratory clinical study of the safety, tolerability and initial efficacy of JY231 injection in the treatment of B-cell acute lymphoblastic leukemia (B-ALL)

Status (registry)
Recruiting
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
20 (estimated)
First submitted
9 Jul 2024
Start date
Jun 2024
Primary completion date
Jun 2026
Lead sponsor
920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
NCT number
NCT06514768

What you commit to

  • Study type: Interventional · Early phase 1
  • Planned participants: 20
  • From Jun 2024 to the primary completion date, Jun 2026
  • 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

  • Previously received treatment targeting CD19;
  • Received autologous hematopoietic stem cell transplantation within 6 weeks;
  • Received other experimental drug treatments within the past 3 months;

Other illness

  • Virological tests of hepatitis B, hepatitis C, AIDS, syphilis and cytomegalovirus were positive;
  • Having a history of other tumors (excluding skin or cervical carcinoma in situ cured by root therapy and without evidence of disease activity);
  • The presence of uncontrollable active bacterial or fungal infections;
  • Allergies to research related drugs or cellular components;
  • Active autoimmune diseases exist;
  • Patients with unstable or active ulcers or gastrointestinal bleeding currently present;
  • Individuals with mental or psychological disorders who cannot cooperate with treatment and efficacy evaluation;
  • Existence of grade II-IV acute graft versus-host disease (GVHD) or widespread chronic GVHD;

Other

  • Pregnant or lactating women, as well as women with pregnancy plans within six months;
  • Researchers believe that other reasons are not suitable for clinical trial participants.

Who the study is looking for

  • up to 75 years (Child, Adult) , either sex;
  • Bone marrow cell morphology examination showed the proportion of primitive and immature lymphocytes in the bone marrow is \>5%, or the bone marrow MRD analysis comfirmed as B-ALL.
  • Flow cytometry or histology confirmed positive expression of cluster of differentiation 19 (CD19);
  • According to the researcher's assessment, the expected survival period is greater than 3 months;
  • Eastern Cooperative Oncology Group (ECOG) physical condition score ≤ 3;
  • The patient has good liver, kidney, heart, and lung functions: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × upper limit of normal(ULN), which can be relaxed to ≤ 5 × ULN for patients with liver invasion; Total serum bilirubin \< 34 μ Mol/L; Creatinine clearance rate\>30 mL/min; Cardiac ejection fraction (EF) ≥ 40%, without pericardial effusion and significant arrhythmia; Indoor oxygen saturation (SpO2) ≥ 92%;
  • Peripheral blood lymphocyte absolute count: absolute lymphocyte count (ALC) ≥ 0.5E9/L, blood platelet (PLT) \> 30E9/L, Hb \> 80g/L, with a single venous access and no other contraindications for blood cell separation;
  • MRI examination showed no active malignant cells in the cerebrospinal fluid, no brain metastases, or no central nervous system leukemia;
  • Individuals with fertility must agree to the use of efficient contraceptive methods;
  • The subject or their legal guardian can understand and voluntarily sign a written informed consent form.

Age in the registry: - to 75 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
920th HJointLogistics
Coordinator of this site? Confirm its status
KunmingChinaRecruiting

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