Annals of Oncology
 2018
DOI: 10.1093/annonc/mdy297.007
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Magnitude 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

M. Borrell Puy
1
,
C. Molto Valiente
2
,
Kerstin Noëlle Vokinger
3
et al.
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