Exploratory Study on Baize DC Injection in Preventing Recurrence and Metastasis After Radical Tumor Surgery

Shanghai Cell Therapy Group

Status and phase

Enrolling

Phase 1

Conditions

Solid Tumor

Treatments

Drug: DC cells

Study type

Interventional

Funder types

Industry

Identifiers

NCT06015269

BZT003-A-01

Details and patient eligibility

About

This is an exploratory study on the safety, immune response, and preliminary effectiveness of single arm, fixed dose therapy

Full description

This study is a clinical study exploring the safety, immune response, and preliminary efficacy of a single arm, 1x107cells dose.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18-80 years old, weight ≥ 40kg; No gender limit;
Subjects with malignant solid tumors diagnosed by histology or cytology and undergoing radical resection surgery;
At the beginning of the study (after surgery), there were no lesions, no local recurrence or distant metastasis on the imaging, and no brain metastasis (images within one month before enrollment can be used for screening);
Subjects in the safety verification stage need to provide immunohistochemical test results with positive expression of Survivin or P53;
ECOG score 0-1 points;
There are sufficient venous channels and no contraindications for peripheral blood mononuclear cell collection surgery;
Organs and bone marrow function well:
1. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50% evaluated by echocardiography within one month of enrollment; The electrocardiogram is basically normal;
2. Platelets ≥ 90 × 10 ^ 9/L;
3. Hemoglobin ≥ 90g/L (no blood transfusion or erythropoietin dependence within 7 days);
4. Total bilirubin ≤ 2 times the upper limit of normal value;
5. Serum creatinine ≤ 1.5 times the upper limit of normal value;
6. Transaminases (AST, ALT) ≤ 2.5 times the upper limit of normal value (if liver cancer is 5 times the upper limit of normal value);
7. International standardized ratio (INR) or prothrombin time (PT) ≤ 1.5 times the upper limit of normal value;
8. Pulmonary function: ≤ CTCAE level 1 dyspnea and SaO2 ≥ 91% in indoor air environment;
Able to understand trial requirements and matters, willing to participate in clinical research according to trial requirements;

Exclusion criteria

HIV and syphilis serological reactions were positive; Hepatitis B surface antigen is positive, hepatitis B core antibody is positive, and the copy number of hepatitis B virus DNA is higher than the lower limit of detection and or greater than or equal to 1000 copies/ml; Or hepatitis C virus infected individuals;
Any uncontrollable active infection, coagulation disorder, or any other major disease;
Pregnant or lactating women
Suffering from active neuroautoimmune or inflammatory diseases, such as any of the following: inflammatory bowel disease, systemic lupus erythematosus, ankylosing spondylitis, scleroderma, multiple sclerosis, Sjogren's syndrome, etc., and receiving relevant treatment; Subjects who are still using immunosuppressants for organ transplantation; Or subjects who have been using immunosuppressive drugs such as glucocorticoids for a long time cannot stop at least 4 weeks before enrollment; Severe allergic constitution;
Subjects with existing abnormalities in the central nervous system, such as seizures, cerebral vascular ischemia/bleeding, dementia, cerebellar diseases, or any autoimmune diseases associated with central nervous system involvement;
Major cardiovascular diseases with clinical significance include:

Symptomatic congestive heart failure

B Unstable angina pectoris

Severe arrhythmia requiring medication treatment

Uncontrolled hypertension

Myocardial infarction or ventricular arrhythmia within 6 months prior to screening
Other situations where researchers believe it is not suitable to participate in clinical trials.