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Virus Therapy
Cohort for Solid Organ Cancer
Phase 1
Waitlist Available
Led By Andrew Brenner, MD
Research Sponsored by Vascular Biogenics Ltd. operating as VBL 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 2 months
Awards & highlights
Study Summary
Aim of the study is to evaluate the safety and find the maximal tolerated dose of VB-111 in Patients with Advanced Metastatic Cancer
Eligible Conditions
- Solid Organ Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Response and progression will be evaluated in this study using the new international criteria proposed by the Response Evaluation Criteria in Solid Tumors (RECIST)
Trial Design
1Treatment groups
Experimental Treatment
Group I: CohortExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ofranergene obadenovec
Not yet FDA approved
Find a Location
Who is running the clinical trial?
Vascular Biogenics Ltd. operating as VBL TherapeuticsLead Sponsor
11 Previous Clinical Trials
1,633 Total Patients Enrolled
Andrew Brenner, MDPrincipal InvestigatorUTHSC- CTRC and Institute for Drug Development
3 Previous Clinical Trials
201 Total Patients Enrolled
Pierre Triozzi, Dr.Principal InvestigatorThe Cleveland Clinic
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