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Topoisomerase I inhibitor
AR-67 for Childhood Gliosarcoma
Phase 2
Waitlist Available
Led By James J Vredneburgh, MD
Research Sponsored by Arno Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 month pfs
Awards & highlights
No Placebo-Only Group
Summary
The primary objective of this study is to determine the 6-month Progression free survival (PFS) when intravenous (IV) AR-67 is administered in adults with confirmed recurrence of GBM who have not recently (\> 90 days) recurred after treatment bevacizumab (including patients who've received temazolamide, but no bevacizumab). The primary objective in the rapid bevacizumab failure group (\< 90 days) is to determine the 2-month PFS.
Eligible Conditions
- Childhood Gliosarcoma
- Glioblastoma
- Gliosarcoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 month pfs
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 month pfs
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Determine the 6-month Progression free survival (PFS) AR-67 is administered in adults with confirmed recurrence of GBM who have not recently (> 90 days) recurred after treatment bevacizumab.
The primary objective in the rapid bevacizumab failure group (< 90 days) is to determine the 2-month PFS.
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: AR-67Experimental Treatment1 Intervention
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Who is running the clinical trial?
Arno TherapeuticsLead Sponsor
7 Previous Clinical Trials
268 Total Patients Enrolled
James J Vredneburgh, MDPrincipal InvestigatorDuke University Medical Center - The Preston Robert Tisch Brain Tumor Center
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