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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01828008
Other study ID # BT-004
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 6, 2013
Last updated April 9, 2013
Start date April 2013
Est. completion date May 2015

Study information

Verified date January 2013
Source Chinese PLA General Hospital
Contact n/a
Is FDA regulated No
Health authority China: General Hospital of PLA
Study type Observational [Patient Registry]

Clinical Trial Summary

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


Description:

Autologous CIK transfusion within 3 days post CD20 antibody treatment.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Han weidong

Outcome

Type Measure Description Time frame Safety issue
Primary disease free survival 5 years Yes
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