“Brief Summary: The study comprises a Phase I component during which the optimal dose of DCVax-Direct for the treatment of solid tissue tumors will be identified, followed by a Phase II component to determine if the injection of DCVax-Direct into selected solid tissue tumors has the ability to reduce tumor growth.”
The primary measure was safety:
“Primary Outcome Measures : Number of patients with adverse events [ Time Frame: 6 months ]
Secondary Outcome Measures : Number of patients with tumor response [ Time Frame: 18 months ]
Other Outcome Measures: Number of patients surviving [ Time Frame: 24 months ] Number of patients surviving without tumor progression [ Time Frame: 24 months ]”