Clinical Trials Directory

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UnknownNCT04209712

Natural Killer Cells Infusion for Treating Acute Myeloid Leukemia Patients With Minimal Residual Disease

Phase I Clinical Trial of Haploid Donor-derived in Vitro Activated Natural Killer Cells Infusion for Patients With Minimal Residual Disease After Consolidation Therapy for Acute Myeloid Leukemia

Status
Unknown
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
6 (estimated)
Sponsor
Shanghai iCELL Biotechnology Co., Ltd, Shanghai, China · Industry
Sex
All
Age
1 Year – 80 Years
Healthy volunteers
Not accepted

Summary

This trial will evaluate the effectiveness and safety of haploid donor-derived in vitro activated natural killer(NK) cells infusion for Treating acute myeloid leukemia Patients With minimal residual disease.

Detailed description

Patients of acute myeloid leukemia after chemotherapy with MRD(minimal residual disease) will receive NK cell infusion combined with consolidation chemotherapy. The bone marrow morphology and MRD remission of the patients will be observed 15 days after the same treatment. All patients will be followed up for 1 year. NK cells are prepared in Beijing iCELL Biotechnology Co.,Ltd, which is subsidiary to Shanghai iCELL Biotechnology Co.,Ltd.

Conditions

Interventions

TypeNameDescription
BIOLOGICALhaploid allogeneic NK cell therapyNK cells will be intravenously infused to the patient for 2 days, with following subcutaneously injection of Interleukin-2.

Timeline

Start date
2020-01-01
Primary completion
2020-12-31
Completion
2021-12-31
First posted
2019-12-24
Last updated
2020-07-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04209712. Inclusion in this directory is not an endorsement.