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A Clinical Research of CD123-Targeted CAR-T in CD123 positive refractory or relapsed Myeloid leukemia

A Clinical Research of CD123-Targeted CAR-T in CD123 positive refractory or relapsed Myeloid leukemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017843
Enrollment
Unknown
Registered
2018-08-17
Start date
2018-08-13
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

CD123 positive refractory or relapsed Acute Myeloid Leukemia

Interventions

case series:CD123+CART -cell

Sponsors

Department of hematology, Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 70 Years

Inclusion criteria

Inclusion criteria: Acute myeloid leukemia (not APL) with recurrence in patients aged 5-70 years (according to 2016 WHO diagnostic criteria) including: 1) Recurrence after hematopoietic stem cell transplantation; 2) Flow cytometric detection of CD123 expression in bone marrow abnormal cells was greater than or equal to 90%; 3) The survival time was expected to be more than 3 months; 4) The activity status score of the eastern United States tumor cooperative group(ECOG) was 0-2 points.

Exclusion criteria

Exclusion criteria: 1) Pregnancy and nursing females; 2) Participation in a prior investigational study within 3 months prior to enrollment; 3) Abnormal liver and kidney function: The definition is that serum aminotransferase and bilirubin are more than 1.5 times the upper limit of normal value; 4) Patients with poor compliance; 5) Other situations we think not eligible for participation in the research; 6) Positive HIV antibodies and syphilis antibodies; 7) Patients with other major diseases; 8) Poor physical condition; 9) Patients with mental illness; 10) Patients with drug abuse or addiction; 11) With serious organ dysfunction and uncontrolled infection.

Design outcomes

Primary

MeasureTime frame
Overall Surviva;Progress Free Survival;Complete Response;minimal residual disease;toxic and adverse effects;

Countries

China

Contacts

Public ContactZhao Mingfeng

Department of hematology, Tianjin First Central Hospital

mingfengzhao@sina.com+86 13752640369

Outcome results

None listed

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