NCT Number: NCT00190424
Randomized Phase 2 With CpG-ODN in Malignant Glioblastoma
The purpose of this study is to determine whether the immunostimulating agent CpG-ODN is effective in the treatment of glioblastoma
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Notify MeKey information
Conditions
Age range
40 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Hopital Lariboisiere, Paris, France
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Glioblastoma
- Karnofsky Performance Status ≥ 60%
Exclusion criteria
- Severe or uncontrolled systemic disease
- Active auto-immune disease
- Uncontrolled epilepsia
- Platelets < 100 000/mm3 ; or Neutrophils <500 /mm3 ; or lymphocytes <300/ mm3
Treatment and study plan
Primary outcomes
-
Survival
Time frame: 2 years
Secondary outcomes
-
Progression-free survival
Time frame: 2 years
-
Tolerance
Time frame: 2 years
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Lead sponsor
Assistance Publique - Hôpitaux de Paris
Other
Registry information
Official study title
Multicentric Randomized Phase 2. Immunotherapy With CpG-ODN in Malignant Glioblastoma
Important dates
- Study start
- 2005
- Primary completion
- 2008
- Study completion
- 2010
- First posted
- Sep 19, 2005
- Registry last updated
- Dec 13, 2012
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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