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Treatment of CIK for Patients With Refractory Non-Hodgkin Lymphoma

S

Soochow University

Status and phase

Not yet enrolling
Phase 2

Conditions

Lymphoma, Non-Hodgkin

Treatments

Biological: Cytokine-induced killer cells (CIK)

Study type

Interventional

Funder types

Other

Identifiers

NCT02497898
RNHL001

Details and patient eligibility

About

The purpose of this study is to study the safety and efficacy of chemotherapy usage followed by CIK transfusion in refractory and/or chemoresistant lymphomas.

Full description

Autologous cytokine-induced killer (CIK) cells transfusion(>2*10^9 cells count) within 2 weeks after regular chemotherapy every 3 months.

Enrollment

1,000 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosed as non-Hodgkin lymphoma with negative effect of regular chemotherapy, and need further therapy

Exclusion criteria

  • patients refuse the therapy or have no tolerance for the therapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,000 participants in 2 patient groups

regular chemotherapy
No Intervention group
Description:
Patients after chemotherapy are just followed up.
CIK regimen
Experimental group
Description:
Patients after chemotherapy will receive at least 3 cycles of Cytokine-induced killer cells (CIK) treatment every 3 months.
Treatment:
Biological: Cytokine-induced killer cells (CIK)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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