An approved in vitro approach to preclinical safety and efficacy evaluation of engineered T cell receptor anti-CD3 bispecific (ImmTAC) molecules

Robust preclinical testing is essential to predict clinical safety and efficacy and provide data to determine safe dose for first-in-man studies. There are a growing number of examples where the preclinical development of drugs failed to adequately predict clinical adverse events in part due to thei...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:PLoS One
Egile Nagusiak: Harper, Jane, Adams, Katherine J., Bossi, Giovanna, Wright, Debbie E., Stacey, Andrea R., Bedke, Nicole, Martinez-Hague, Ruth, Blat, Dan, Humbert, Laure, Buchanan, Hazel, Le Provost, Gabrielle S., Donnellan, Zoe, Carreira, Ricardo J., Paston, Samantha J., Weigand, Luise U., Canestraro, Martina, Sanderson, Joseph P., Botta Gordon-Smith, Sophie, Lowe, Kate L., Rygiel, Karolina A., Powlesland, Alex S., Vuidepot, Annelise, Hassan, Namir J., Cameron, Brian J., Jakobsen, Bent K., Dukes, Joseph
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2018
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6188753/
https://ncbi.nlm.nih.gov/pubmed/30321203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0205491
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