1563PDMagnitude of clinical benefit in trials supporting US Food and Drug Administration (FDA) accelerated approval (AA) and European Medicines Agency (EMA) conditional marketing authorisation (CMA) and subsequent trials supporting conversion to full approval

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Veröffentlicht in:Annals of oncology 2018-10, Vol.29 (suppl_8)
Hauptverfasser: Borrell Puy, M, Molto Valiente, C, Vokinger, K, Hwang, T, Ocana Fernandez, A, Templeton, A J, Seruga, B, Gich Saladich, I, Barnadas, A, Amir, E, Tibau, A
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container_title Annals of oncology
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creator Borrell Puy, M
Molto Valiente, C
Vokinger, K
Hwang, T
Ocana Fernandez, A
Templeton, A J
Seruga, B
Gich Saladich, I
Barnadas, A
Amir, E
Tibau, A
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doi_str_mv 10.1093/annonc/mdy297.007
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title 1563PDMagnitude of clinical benefit in trials supporting US Food and Drug Administration (FDA) accelerated approval (AA) and European Medicines Agency (EMA) conditional marketing authorisation (CMA) and subsequent trials supporting conversion to full approval
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