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CCCR-NK92 Cells Immunotherapy for Non-small Cell Lung Carcinoma

X

Xinxiang medical university

Status and phase

Completed
Phase 1

Conditions

Non-small Cell Lung Cancer

Treatments

Biological: CCCR-NK92 cells

Study type

Interventional

Funder types

Other

Identifiers

NCT03656705
CNK-101

Details and patient eligibility

About

The purpose of this clinical investigation is to evaluate the safety and effects of CCCR-modified NK92(CCCR-NK92)infusions in previously treated advanced non-small cell lung carcinoma(NSCLC).

Enrollment

2 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1.Male and female subjects with non-small cell lung carcinoma in patients with no available curative treatment options who have limited prognosis(≧3 months)with currently available therapies will be enrolled.
  • 2.The last cytotoxic drug, radiotherapy or surgery≧4 weeks.
  • 3.HB≧90g/L, ANC≧1.5×10e9/L, PLT≧80×10e9/L, TBIL≦1.5×upper limit of nomal, ALT/AST≦2.5×upper limit of nomal, ALT/AST≦5×upper limit of nomal if have liver metastasis, Cr≦1.5×upper limit of nomal or CCr≧60ml/min.

Exclusion criteria

  • 1.Pregnancy or breastfeeding.
  • 2.Known HIV, HBV or HCV infection.
  • 3.Active antoimmune disease.
  • 4.History of severe immediate hypersensitivity to any of the biological products including penicillin.
  • 5.Severe psychiatric disorder which might interfere with the study treatment or examination.
  • 6.Chronic heart failure NYHA≧III.
  • 7.Simultaneous participation in another clinical trial within 4 weeks.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2 participants in 1 patient group

CCCR-NK92 cells immunotherapy
Experimental group
Description:
Preparation of CCCR-NK92 cells suspended in a saline and plasma solution.
Treatment:
Biological: CCCR-NK92 cells

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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