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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03152708
Other study ID # CAN-B1-008-L-009
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 11, 2017
Last updated September 20, 2017
Start date November 1, 2017
Est. completion date December 31, 2017

Study information

Verified date September 2017
Source CANbridge Life Sciences Ltd.
Contact Jack Hou
Phone 00862152996609
Email jhou@canbridgepharma.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study was conducted on the post-operative tumor tissues from 62 GBM patients. 20 slices are necessary for all the CD95 and CpG2 test in the central lab by the methods of immunisation and DNA methylation.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 62
Est. completion date December 31, 2017
Est. primary completion date December 1, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Chinese nationality

- No limits on Gender and age

- First diagnosed GBM

- Brain tumor tissue cytological diagnosis of glioblastoma (GBM, pleomorphic glioblastoma, WHO level IV)

Exclusion Criteria:

- Other types of glioma by histological diagnosis

- Tumor tissue not eligible for the central laboratory testing standard

- No enough tumor tissue for the central laboratory test

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
CANbridge Life Sciences Ltd.

Outcome

Type Measure Description Time frame Safety issue
Primary CD95 Ligand Positive Rate 0 day
Secondary CpG2 Positive Rate 0 day
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