Clinical Trials Directory

Trials / Completed

CompletedNCT01582516

Safety Study of Replication-competent Adenovirus (Delta-24-rgd) in Patients With Recurrent Glioblastoma

A Phase I/II Trial of a Conditionally Replication-competent Adenovirus (Delta-24-rgd) Administered by Convection Enhanced Delivery in Patients With Recurrent Glioblastoma

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Erasmus Medical Center · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

In the Netherlands a 2 center investigator-driven phase I/II clinical trial is initiated in June 2010 testing the oncolytic adenovirus Delta24-RGD to treat glioblastoma patients. The virus is administrated using convection-enhanced delivery by 4 catheters as delivery technique, targeting solid tumor as well as infiltrated tumor cells within the peri-tumoral brain. Patients will be enrolled in cohorts of 3 per dose-level. The dose levels to be explored are: 10\^7, 10\^8, 10\^9, 10\^10, 3\*10\^10 and 10\^11 viral particles (vp). Once the MTD has been determined, or the study has reached the highest dose cohort, a further 6 or 9 patients will be enrolled at the MTD and evaluated for safety and preliminary signs of efficacy, such that in total at least 12 patients have received the MTD. The primary objective is to determine the safety and tolerability of Delta-24-RGD administered by CED to the tumor and the surrounding infiltrated brain in patients with recurrent GBM. Secondary objectives are to determine the Progression Free Survival (PFS), Overall Survival (OS), and tumor response rate in patients with recurring tumors amenable for surgical resection and treated at the MTD. Cerebrospinal fluid as well as brain interstitial fluid by microdialysis next to the routinely collected samples of blood at various timepoints before, during and after virus infusion. Various neurodegenerative biomarkers as well as markers of immune response will be assessed in these samples. Furthermore extensive sampling and PCR analyses will be performed to evaluate distribution and shedding of the virus.

Conditions

Interventions

TypeNameDescription
BIOLOGICALdelta-24-RGD adenovirusslow continuous microinfusion in and around the brain tumor during 44 hrs.by 4 temporary placed catheters

Timeline

Start date
2010-06-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2012-04-20
Last updated
2015-03-09

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01582516. Inclusion in this directory is not an endorsement.