67
Participants
Start Date
February 29, 2000
Primary Completion Date
August 31, 2015
Study Completion Date
October 31, 2015
AV0113 DC-CIT
Mature loaded DCs will be injected intra-nodally into tumour free lymph nodes or subcutaneously close to tumour free lymph nodes at weekly intervals for at least 6 weeks.
Data evaluation
"For obtaining a clearer picture of AV0113's utility in the treatment of bone and soft tissue sarcoma, a LT follow-up investigation of the 14 Sarcoma patients, which will be treated using the AV0113 DC-CIT technology, is planned, in order to gather first evidence for a potential LT effect of DC-CIT with AV0113.~Furthermore, a comparison of the 14 sarcoma patients treated with AV0113 DC-CIT with a cohort of matched historic control patients that were treated using standard of care will be conducted. It is planned to analyse 42 control sarcoma patients that will be matched for disease, recurrences, relapses etc"
Department of Orthopaedics, Medical University Vienna, Vienna
St. Anna Children's Hospital, Vienna
Lead Sponsor
Activartis Biotech
INDUSTRY