CAR-T Technology for Recurrent/Refractory Malignant Hematological and Lymphatic Tumors

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age14-75
SponsorMingzhi Zhang

About this trial

evaluate the safety and Esfficacy of CAR-T technology for the treatment of recurrent/refractory malignant hematological lymphomas

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The participant has given informed consent and signed the consent form, and is willing and capable of complying with the scheduled visits, study treatment, laboratory examinations, and other trial procedures.

Anti-CD20 monoclonal antibodies

Combination chemotherapy containing anthracyclines.

Age 14-75 years (inclusive), both male and female.

Disqualifiers

History of any of the following cardiovascular diseases within the past 6 months: New York Heart Association (NYHA) class III or IV heart failure, cardiovascular intervention (angioplasty or stenting), myocardial infarction, unstable angina, or other clinically significant heart diseases.

History of severe pulmonary dysfunction.

Concurrent advanced malignant tumors.

Concurrent systemic fungal, bacterial, viral, or other infections that cannot be effectively controlled.

Trial design

Design model

Single group

Treatments tested in this trial

  • CAR-T Therapy

    Biological/Vaccine

    CAR-T Technology for the Treatment of Recurrent/Refractory Malignant Hematological Lymphomas

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: TreatmentExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

objective response rate(ORR)

evaluate the efficacy of CAR-T cell infusion for the treatment of relapsed/refractory malignant hematological tumors

Time frame
6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Mingzhi Zhang

Lead sponsor

Zhengzhou University

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: