Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/96528
Title: Outcomes and endpoints in clinical trials supporting the marketing authorisation of treatments in paediatric acute lymphoblastic leukaemia
Authors: Micallef, Benjamin
Nistico, Robert
Bjerrum, Ole Weis
Sarac, Sinan Bardakci
Butler, Dianne
Serracino-Inglott, Anthony
Borg, John Joseph
Keywords: Cancer research
Human genetics
Lymphoblastic leukemia
Lymphoblastic leukemia in children
Lymphoblastic leukemia in children -- Treatment
Issue Date: 2022
Publisher: Elsevier
Citation: Micallef, B., Nistico, R., Bjerrum, O. W., Sarac, S. B., Butler, D., Serracino-Inglott, A., & Borg, J. J. (2022). Outcomes and endpoints in clinical trials supporting the marketing authorisation of treatments in paediatric acute lymphoblastic leukaemia. Drug Discovery Today. In press. DOI:https://doi.org/10.1016/j.drudis.2022.05.015
Abstract: The improvement in acute lymphoblastic leukaemia (ALL) treatment has led research efforts to focus on the unmet medical needs of an increasingly smaller patient cohort with resistant leukaemia and to develop more-targeted agents. Survival and response rates remain the most-prevalent endpoints in paediatric ALL research, but other intermediate clinical endpoints and molecular biomarkers for efficacy and mid- and long-term safety endpoints are also being investigated. The success of current ALL treatment appears to be driving new paradigms to optimise clinical drug development, while at the same time, regulatory tools in place are supporting meaningful drug development in the area.
URI: https://www.um.edu.mt/library/oar/handle/123456789/96528
Appears in Collections:Scholarly Works - FacM&SPha



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