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Full notification Final report - General information Notification Number B/DE/22/PEI4746 Member State to which the notification was sent Germany Date of acknowledgement from the Member State Competent Authority 15/12/2021 Title of the Project PHE885 – Autologous genetically modified T cells, intravenous administration. Treatment of relapsed/refractory malignancies Proposed period of release: 25/08/2022 to 11/06/2025 Name of the Institute(s) or Company(ies) Novartis Pharma AG, Postfach, 4002 Basel, Switzerland
Is the same GMO been notified elsewhere by the same notifier? Yes:
Germany; Spain; France; United Kingdom; Greece; Italy;
Has the same GMO been notified elsewhere by the same notifier? No GMO characterization GMO is a: Other Identity of the GMO: Autologous T cells transduced with a replication-deficient HIV-1 derived viral vector to express a chimeric (murine/human) antigen receptor (CAR). Information relating to the recipient or parental organisms from which the GMO is derived Common Name: Human Genus: Homo Species: Subspecies: Strain: Pathovar: European Commission administrative Information Consent given by the Member State Competent Authority: Not known
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