drugset / Trial / NCT00045968

Study of a Drug [DCVax®-L] to Treat Newly Diagnosed GBM Brain Cancer

NCT00045968

Phase 3 Unknown 348 enrolled Northwest Biotherapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of the study is to determine the efficacy of an investigational therapy called DCVax(R)-L in patients with newly diagnosed GBM for whom surgery is indicated. Patients must enter screening at a participating site prior to surgical resection of the tumor. Patients will receive the standard of care, including radiation and Temodar therapy and two out of three will additionally receive DCVax-L, with the remaining one third receiving a placebo. All patients will have the option to receive DCVax-L in a crossover arm upon documented disease progression. (note: DCVax-L when used for patients with brain cancer is sometimes also referred to as DCVax-Brain)

Timeline

Start
2006-12
Primary completion
2022-11
Completion

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator DCVax-L Vaccine Other