Skip to content

A clinical study on the treatment of relapsed and refractory acute myeloid leukemia with universal double negative T cells

A clinical study on the treatment of relapsed and refractory acute myeloid leukemia with universal double negative T cells

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063021
Enrollment
Unknown
Registered
2022-08-28
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed and refractory acute myeloid leukemia

Interventions

Group 1 :Infusion DNT

Sponsors

The First Affiliated Hospital of School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Understand and voluntarily sign the informed consent; 2. Age: 18-75 years old; 3. According to the 2016 WHO diagnostic criteria for AML, patients diagnosed as AML other than acute promyelocytic, who have achieved complete remission after 2 courses of regular treatment or have achieved complete remission after previous treatment, but the latest assessment suggests disease recurrence.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with acute promyelocytic leukemia; 2. It is known that there is persistent infection within 3 days and needs to receive systemic treatment; 3. Subjects known to have active central nervous system leukemia; 4. Within the first 3 days of infusion of DNT cells, the subject was treated with Cox2 inhibitors and glucocorticoids; 5. Patients who are allergic to immunotherapy or related drugs; 6. Patients with heart disease >= 2 NYHA grade or high blood pressure that is difficult to control and need treatment; 7. Patients who have previously received organ transplants or are about to receive organ transplants (except bone marrow or hematopoietic stem cell transplants); 8. Patients who have been judged by the investigator to be unsuitable for participating in this study.

Design outcomes

Primary

MeasureTime frame
Response rate;

Secondary

MeasureTime frame
safety;Disease free survival;Relapse free survival;Overall survival;

Countries

China

Contacts

Public ContactCai Zhen

The First Affiliated Hospital of School of Medicine, Zhejiang University

Caiz1@zju.edu.cn+86 13657190311

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026