Full notification file
General informationNotification NumberB/HU/13/01Member State to which the notification was sentHungaryDate of acknowledgement from the Member State Competent Authority03/04/2013Title of the ProjectA Phase 2b, Double-Blind, Placebo-Controlled, Multinational, Multicenter, Randomized Study Evaluating the Safety and Efficacy of Intracoronary Administration of MYDICAR® (AAV1/SERCA2a) in Subjects with Heart Failure.Proposed period of release:01/07/2013 to 30/09/2013Name of the Institute(s) or Company(ies)Celladon Corporation, ;
3. Is the same GMO release planned elsewhere in the Community?NoHas the same GMO been notified elsewhere by the same notifier?YesIf yes, notification number(s): B/BE/12/BVW2; GMO characterizationGMO is a:DNA VirusIdentity of the GMO:Genus: Dependovirus
Species: Adeno-associated virus (vector). The AAV1/SERCA2a vector is a recombinant adeno-associated virus (rAAV) vector. It is a pseudotype of AAV serotype 1(AAV1) and is denoted as rAAV1/2. As such, the capsid proteins are from wt AAV1 and the AAV DNA (two 148 base inverted terminal repeats) is from wtAAV2Information relating to the recipient or parental organisms from wich the GMO is derived| Common Name | Genus | Species | Subspecies | Strain | Pathovar | | AAV1 | Dependovirus | Adeno-associated Virus | N/A | Serotype 1 | N/A |
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European Commission administrative informationConsent given by the Member State Competent Authority:Not known