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Treatment of CD20 Antibody Plus CIK for Patients With Refractory Lymphomas

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01828008
Acronym
CIK
Enrollment
20
Registered
2013-04-10
Start date
2013-04-30
Completion date
2015-05-31
Last updated
2013-04-10

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

Conditions

Lymphomas

Keywords

Mabthera, cytokine induced killer cell

Brief summary

To study the safety and efficacy of CD20 antibody usage followed by CIK transfusion in refractory and/or chemoresistant lymphomas.

Detailed description

Autologous CIK transfusion within 3 days post CD20 antibody treatment.

Interventions

None listed

Sponsors

Han weidong
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

\- diagnosed as B-cell lymphoma with CD20 positiveness, and need to therapy

Exclusion criteria

\- to refuse the therapy and need not tolerate the therapy

Design outcomes

Primary

MeasureTime frame
disease free survival5 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026