drugset / Trial / NCT01470794

Study of a Retroviral Replicating Vector Combined With a Prodrug to Treat Patients Undergoing Surgery for a Recurrent Malignant Brain Tumor

NCT01470794

Phase 1 Completed 58 enrolled Tocagen Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter study evaluating the safety and tolerability of increasing doses of Toca 511, a retroviral replicating vector, injected into the resection cavity of patients with Grade III or Grade IV Gliomas who have elected to undergo surgical removal of their tumor. Approximately 6 weeks after injection of Toca 511, patients will begin an oral courses of Toca FC, an antifungal agent. These one week courses of Toca FC will be repeated during the approximately 30 week study. Two separate cohorts of patients treated with Toca 511 and Toca FC will also be evaluated with either of the following standard treatments for glioma: lomustine or bevacizumab. After completion of this study, all patients will be eligible for enrollment and encouraged to enter a long-term continuation protocol that enables additional Toca FC treatment cycles to be given, as well as permits the collection of long-term safety and survival data.

Timeline

Start
2012-02
Primary completion
2016-04-12
Completion
2016-04-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Flucytosine Small molecule Oral
Subject Vocimagene Amiretrorepvec Unknown Other