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

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
AgeUp to 75
Sponsor920th Hospital of Joint Logistics Support Force of People's Liberation Army of China

About this trial

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)

Eligibility criteria

Qualifiers

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;

Disqualifiers

Pregnant or lactating women, as well as women with pregnancy plans within six months;

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);

Previously received treatment targeting CD19;

Trial design

Treatments tested in this trial

  • JY231

Treatment groups

20 Participants
are divided into 1 treatment group