Clinical Study of Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of Myeloid Leukemia

Acute Myeloid Leukemia Clinical Trial

Official title:

Clinical Study of Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of Myeloid Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04923919
• Other study ID #: BG-CT-19-005
• Status: Recruiting
• Phase: Early Phase 1
• Start date: September 14, 2021
• Est. completion date: December 5, 2024

Study information

• Verified date: July 2023
• Source: 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
• Contact: Wang Sanbin, Doctor
• Phone: (86)13187424131
• Email: Sanbin1011[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Researchers plan to enroll a total of 100 patients with relapsed, refractory acute myeloid leukemia (AML) to receive a single dose of autologous CAR T cells.The safety of CAR T therapy was evaluated by observing adverse events after cell therapy;The efficacy of CAR-T therapy was evaluated against the outcome of patients' own past standard treatment regimens or historical data.Blood and bone marrow were collected before and 12 months after infusion to detect the number and activity of CAR T cells, and to evaluate the pharmacokinetics (PK) of CAR T cells.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: December 5, 2024
• Est. primary completion date: December 5, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 75 Years

Eligibility

Inclusion Criteria:

1. The diagnosis of myeloid leukemia was clear;Refractory treatment was defined as: (1) 2 patients who did not achieve partial remission after treatment with standard induced remission regimens.? The patients who relapsed within 6 months after the first remission were also called early recurrence.? The failure relapsed 6 months after the initial response, but was retreated with the original induced response regimen.(4) multiple relapse.Relapse is defined as: patients who achieve complete remission after treatment, more than 5% of leukemia cells in the bone marrow, also known as intramedullary recurrence;Or the presence of leukaemia outside the bone marrow, also known as extramedullary relapse (usually in the central nervous system, testicular leukemia is the most common);

2. Diseased cells were confirmed to express CD123, CLL1 and other targets;

3. KPS > 60 points;

4. Expected survival of more than 3 months;

5. No gender limitation, age 2-75;

6. Patients clinically diagnosed as high-risk type, refractory type of recurrence or not eligible for standard treatment;

7. No serious mental disorders;

8. Sufficient heart, liver and renal function (a. Liver function: ALT/AST < 3 times upper limit of normal value (ULN) and bilirubin =34.2µmol/L;B. Renal function: creatinine < 220µmol/L;C. Lung function: indoor oxygen saturation =95%;D. Cardiac function: left ventricular ejection fraction (LVEF) =40%;);

9. No other serious diseases (such as autoimmune diseases, immune deficiency, organ transplantation) that are in conflict with this program;

10. Can cooperate with trial management and follow-up;

11. Patients voluntarily participated in the study and signed the informed consent

Exclusion Criteria:

1. History of other malignant tumors;

2. Uncontrolled active infection;

3. Patients with underlying diseases requiring systemic use of glucocorticoids;

4. Acute or chronic GVHD;

5. T-cell inhibitor therapy;

6. Pregnant and lactating women;

7. Patients with active hepatitis B;

8. Other conditions considered by the investigator to be inappropriate for the study (HIV infection, intravenous drug addiction, etc.), or other conditions that may affect the analysis of the results of the clinical study.

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• Leukemia
• Leukemia, Myeloid

Intervention

Drug:
• Anti-CLL1 CART cells
In this study, patients with acute myeloid leukemia were treated with autologous anti-CLL1 CAR T cells by a single, intravenous infusion.Blood and bone marrow were collected before and 12 months after infusion to detect the number and activity of CAR T cells, and to evaluate the efficacy of CAR T cells.

Locations

Country	Name	City	State
China	No.212 Daguan Road, Xishan District	Kunming	Yunnan

Sponsors (1)

Lead Sponsor	Collaborator
920th Hospital of Joint Logistics Support Force of People's Liberation Army of China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of AE after CAR-T infusion	Incidence of adverse events after CAR-T infusion; Data. The records of adverse events (AE) should include: description of AE and all related symptoms, occurrence time, severity, duration, measures taken, final results and outcomes. According to NCI CTC AE 5.0 standard, AE was scored; Grade.; Safety evaluation indexes include but are not limited to the following contents; Any spontaneously reported and all directly observed adverse events; Any abnormal changes in vital signs and physical examination; The abnormal results of laboratory examination, physical examination and blood examination with clinical significance after treatment	up to 12 months after CAR-T infusion
Secondary	ORR rate	Overall response rate (ORR=CR+CRi) after CAR-T infusion	1month, 2 months, 3months, 6months ,12months after CAR-T infusion
Secondary	PFS	Progression free survival (PFS) after CAR-T infusion	1month, 2 months, 3months, 6months ,12months after CAR-T infusion
Secondary	OS	overall survival (OS) after CAR-T infusion	1month, 2 months, 3months, 6months ,12months after CAR-T infusion
Secondary	Change of CAR Copies	CAR Copies measured by qPCR after CAR-T infusion	Days 4, 7, 10, 14 and months 2, 3, 6, 9, 12 after Fast Dual CAR-T infusion
Secondary	Change of CAR-T cell counts	CAR-T cell counts measured by Flow cytometry after CAR-T infusion	Days 4, 7, 10, 14 and months 2, 3, 6, 9, 12 after Fast Dual CAR-T infusion