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Treatment of patients with leukemia using NK cells

A Clinical trial to assess the effect of Natural Killer Cell transplantation in treatment of patients with Acute lymphoblastic leukemia (ALL) and chronic lymphocytic leukemia (CLL)

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017083027520N9
Enrollment
10
Registered
2017-10-19
Start date
2017-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Acute lymphoblastic leukemia (ALL). Condition 2: Chronic lymphocytic leukemia (CLL). Acute lymphoblastic leukaemia Chronic lymphocytic leukaemia

Interventions

Injecting 29 * 106 /kg NK cells to patients with leukemia Intravenously and then Injection of Repetitive doses of IL-2 (6 doses) subcutaneously to stimulate the proliferation and activation of NK-posi
Treatment - Other

Sponsors

Stem Cell And Regenerative Medicine Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-Age range of 18- 25 years for ALL patients; 2-Age range over 50 years for patients with CLL; 3- Those who have a proper cell donors with incongruent KIR (Haploidentical KIR-L mismatched donor); 4- Patients with adequate organ function; 5-Access to the patient for the continuation of treatment and follow-up (preferably from Azeri-speaking patients for easier access and removal of the Zentique variable); Exclusion criteria : 1-Patients with active and uncontrolled infections; 2-Abnormal kidney, lung and liver function, measured by serum creatinine (serum creatinine> 2 mg / dl), saturated oxygen O2 = 96%) (Sat and liver enzymes (ALT / AST> 2.5 x N); 3-Patients with Down syndrome; 4- Patients with acute promyelocytic leukemia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Phenotype and function of NK cells. Timepoint: 2, 7, 14, 21 and 28 days after the transplant. Method of measurement: Flow cytometry.

Secondary

MeasureTime frame
IFN?. Timepoint: 2, 7, 14, 21 and 28 days after the transplant. Method of measurement: Flow cytometry.;CD107. Timepoint: 2, 7, 14, 21 and 28 days after the transplant. Method of measurement: Flow cytometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeili Aghebati Maleki

Stem Cell And Regenerative Medicine Institute

leili_aghebati_maleki@yahoo.com+98 41 3336 4665

Outcome results

None listed

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