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Exploration of the antibody–drug conjugate clinical landscape

The antibody–drug conjugate (ADC) field has undergone a renaissance, with substantial recent developmental investment and subsequent drug approvals over the past 6 y. In November 2022, Elahere(TM) became the latest ADC to be approved by the US Food and Drug Administration (FDA). To date, over 260 AD...

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Detalles Bibliográficos
Autores principales: Maecker, Heather, Jonnalagadda, Vidya, Bhakta, Sunil, Jammalamadaka, Vasu, Junutula, Jagath R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464553/
https://www.ncbi.nlm.nih.gov/pubmed/37639687
http://dx.doi.org/10.1080/19420862.2023.2229101
Descripción
Sumario:The antibody–drug conjugate (ADC) field has undergone a renaissance, with substantial recent developmental investment and subsequent drug approvals over the past 6 y. In November 2022, Elahere(TM) became the latest ADC to be approved by the US Food and Drug Administration (FDA). To date, over 260 ADCs have been tested in the clinic against various oncology indications. Here, we review the clinical landscape of ADCs that are currently FDA approved (11), agents currently in clinical trials but not yet approved (164), and candidates discontinued following clinical testing (92). These clinically tested ADCs are further analyzed by their targeting tumor antigen(s), linker, payload choices, and highest clinical stage achieved, highlighting limitations associated with the discontinued drug candidates. Lastly, we discuss biologic engineering modifications preclinically demonstrated to improve the therapeutic index that if incorporated may increase the proportion of molecules that successfully transition to regulatory approval.