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• W4313458182 abstract "The recent success of antibody-drug conjugates (ADC), exemplified by seven new FDA-approvals within three years, has led to increased attention for antibody based targeted therapeutics and fueled efforts to develop new drug-linker technologies for improved next generation ADCs. We present a highly efficient phosphonamidate-based conjugation handle that combines a discrete hydrophilic PEG-substituent, an established linker-payload and a cysteine-selective electrophile in one compact building block. This reactive entity provides homogeneous ADCs with a high drug-to-antibody ratio (DAR) of 8 in a one-pot reduction and alkylation protocol from non-engineered antibodies. The compact branched PEG-architecture introduces hydrophilicity without increasing the distance between antibody and payload, allowing the generation of the first homogeneous DAR 8 ADC from VC-PAB-MMAE without increased in vivo clearance rates. This high DAR ADC exhibits excellent in vivo stability and increased antitumor activity in tumour xenograft models relative to the established FDA approved VC-PAB-MMAE ADC Adcetris, clearly showing the benefit of the phosphonamidate based building-blocks as a general tool for the efficient and stable antibody-based delivery of highly hydrophobic linker-payload systems." @default.
• W4313458182 created "2023-01-06" @default.
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• W4313458182 date "2023-01-01" @default.
• W4313458182 modified "2023-10-14" @default.
• W4313458182 title "Compact hydrophilic electrophiles enable highly efficacious high DAR ADCs with excellent <i>in vivo</i> PK profile" @default.
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• W4313458182 doi "https://doi.org/10.1039/d2sc05678j" @default.
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• W4313458182 hasPublicationYear "2023" @default.
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