Full notification file
Member State to which the notification was sent
Date of acknowledgement from the Member State Competent Authority
Title of the Project
Clinical Study BNIT-PRV-301, "A Randomized, Double-blind, Phase 3 Efficacy Trial of PROSTVAC ± GM-CSF in Men With Asymptomatic or Minimally Symptomatic Metastatic, Castrate-Resistant Prostate Cancer"
Proposed period of release:
01/01/2012 to 30/05/2012
Name of the Institute(s) or Company(ies)
BN ImmunoTherapeutics, Inc., ;
3. Is the same GMO release planned elsewhere in the Community?
Has the same GMPt been notified elsewhere by the same notifier?
If yes, notification number(s):
GMO is a:
Identity of the GMO:
PROSTVAC-V/F is a live attenuated viral vector-based investigational vaccine product that is comprised of two component viral vectors, to be used together in a prime-boost vaccination regimen: (1) PROSTVAC-V: Recombinant vaccinia virus that contains a modified gene encoding human prostate-specific antigen (PSA) and genes encoding three human immunological costimulatory molecules: B7.1, intracellular adhesion molecule-1 (ICAM-1), and leukocyte function-associated antigen-3 (LFA-3) (or TRIad of COstimulatory Molecules, TRICOM™); and (2) PROSTVAC-F: Recombinant fowlpox virus that co-expresses the same four human genes as PROSTVAC-V.
PROSTVAC-V: Genus: Orthopox Virus
PROSTVAC-F : Genus: Avipox Virus
Information relating to the recipient or parental organisms from wich the GMO is derived
New York City Board of Health Vaccine
European Commission administrative information
Consent given by the Member State Competent Authority:
Consent given for trial of 2 vaccines against prostate cancer, developed using a modified attenuated vaccinia virus and a modified fowl pox virus. The applicants anticipate trials in the EU will take place between January 2012 and October 2013. This consent covers 10 hospital and clinic sites in England.