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Report No. 3 on the progress of the clinical evaluation of the EudraCT project 2018-004789-32, code UHKT-CAR19-01, 9.6.2022 - 8.6.2023: Development Safety Update Report: Development Safety Update Report 2023: Safety and efficacy of anti-CD19 chimeric antigen receptor-modified autologous T cells (CART19) in patients with relapsed/refractory CD19+ acute lymphoblastic leukemia and non-Hodgkin lymphoma. A dose escalation, open-label, phase I study. (2023)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A90249%2F23%3A00135351" target="_blank" >RIV/00216224:90249/23:00135351 - isvavai.cz</a>

  • Result on the web

    <a href="https://test.uhkt.cz/clinical-trials/clinical-trials" target="_blank" >https://test.uhkt.cz/clinical-trials/clinical-trials</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Report No. 3 on the progress of the clinical evaluation of the EudraCT project 2018-004789-32, code UHKT-CAR19-01, 9.6.2022 - 8.6.2023: Development Safety Update Report: Development Safety Update Report 2023: Safety and efficacy of anti-CD19 chimeric antigen receptor-modified autologous T cells (CART19) in patients with relapsed/refractory CD19+ acute lymphoblastic leukemia and non-Hodgkin lymphoma. A dose escalation, open-label, phase I study. (2023)

  • Original language description

    Report No. 3 on the progress of the clinical evaluation of the EudraCT project 2018-004789-32, code UHKT-CAR19-01, 9.6.2022 - 8.6.2023: Development Safety Update Report: Development Safety Update Report 2023: Safety and efficacy of anti-CD19 chimeric antigen receptor-modified autologous T cells (CART19) in patients with relapsed/refractory CD19+ acute lymphoblastic leukemia and non-Hodgkin lymphoma. A dose escalation, open-label, phase I study. (2023) Report No. 3 was prepared on the progress of the clinical evaluation 9/6/2022 - 8/6/2023: Development Safety Update Report 2023: Safety and efficacy of anti-CD19 chimeric antigen receptor-modified autologous T cells (CART19) in patients with relapsed/refractory CD19+ acute lymphoblastic leukemia and non-Hodgkin lymphoma. A dose escalation, open-Iabel, phase I study: EudraCT project 2018-004789-32, code UHKT-CAR19-01.

  • Czech name

  • Czech description

Classification

  • Type

    V<sub>souhrn</sub> - Summary research report

  • CEP classification

  • OECD FORD branch

    30230 - Other clinical medicine subjects

Result continuities

  • Project

  • Continuities

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Number of pages

    4

  • Place of publication

    Praha

  • Publisher/client name

    ÚHKT PRAHA

  • Version