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Status unknownNCT03152708Updated Sep 21, 2017

CAN008 Biomarker CD95 Ligand and CpG2 Methylation in Chinese Patients With Glioblastoma

An observational study in Glioblastoma, sponsored by CANbridge Life Sciences Ltd.. Status unknown. Per ClinicalTrials.gov, last updated 2017-09-21.

Sponsored by CANbridge Life Sciences Ltd. · Observational

The sponsor has not verified this record recently (last verified Sep 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
62
Sex
All
01

Study 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.

02

Conditions studied

  • Glioblastoma

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03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Chinese GBM patients

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

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
04

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
62 participants (estimated)
Patient registry
No
05

What researchers measure

Primary outcomes

  1. CD95 Ligand Positive Rate

    Time frame: 0 day

Secondary outcomes

  1. CpG2 Positive Rate

    Time frame: 0 day

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Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03152708
Lead sponsor
CANbridge Life Sciences Ltd.
Responsible party
Sponsor
First posted
May 15, 2017
Start date
Nov 1, 2017 (estimated)
Primary completion
Dec 1, 2017 (estimated)
Completion
Dec 31, 2017 (estimated)
Last update
Sep 21, 2017

Study contacts

Jack Hou
Contact
jhou@canbridgepharma.com
00862152996609
Jinsong Wu, MD
principal investigator · Huashan Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

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