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Safety of cell immunotherapy for refractory malignant tumor using natural killer cell-like effector cells (CA-MED-NK001) selectively amplified from autologous mononuclear cells in peripheral blood

Phase 1
Conditions
all classes of malignant tumors, after treatment with (or not applicable for) standard therapies for cancers
Registration Number
JPRN-UMIN000015733
Lead Sponsor
Center for Advanced Medical Innovation, Kyushu University
Brief Summary

This trial has been terminated due to the difficulties of the recruitment of condition-matched subjects after the entry of four patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

Patients to be excluded would satisfy any of the following conditions: (1) pulmonary fibrosis and/or interstitial pneumonia (2) patients who have a history of severe drug allergy (3) serum positive for HBs antigen, HCV, HTLV-1 and/or HIV antibody (4) active autoimmune disease (5) patients who are taking steroids and/or immunosuprresive agents (6) double or more cancers (7) uncontrolable infectious disease (8) Patients to be or wishing for pregnancy, or breast-feeding (9) T cell- or NK cell-originated leukemia and/or lymphoma (10) heavy cardiological disease (11) Patientss who are regarded as inadequate for study enrollment by the investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safety (Adverse events and their frequency, timing, duration and incidence rate)
Secondary Outcome Measures
NameTimeMethod
Efficacy and immunological response
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